Matrix_101 | ERF5 | Not available | Upstream | -137 |
Matrix_108 | PIF4 | Interaction between BZR1 and PIF4 integrates brassinosteroid and environmental responses | Upstream | -435 |
| | | Upstream | -429 |
Matrix_110 | ATABI4;AT3G57600 | Not available | Upstream | -139 |
Matrix_118 | PIF3_2 | Direct targeting of light signals to a promoter element-bound transcription factor | Upstream | -432 |
Matrix_120 | BEE2 | Not available | Upstream | -428 |
Matrix_122 | ABF1;AREB2 | Not available | Upstream | -429 |
Matrix_130 | TCP16 | Not available | Upstream | -569 |
Matrix_138 | RRTF1 | Not available | Upstream | -138 |
Matrix_14 | ZCW32;AT5G62610 | Not available | Upstream | -434 |
| | | Upstream | -427 |
Matrix_144 | AT5G08330;AT5G23280 | Not available | Upstream | -569 |
| | | Upstream | -568 |
Matrix_146 | ORA47 | Not available | Upstream | -137 |
Matrix_147 | ERF3;AT1G80580 | Not available | Upstream | -137 |
Matrix_15 | PIF3_1 | Direct targeting of light signals to a promoter element-bound transcription factor | Upstream | -641 |
Matrix_150 | UNE10;PIF7 | Not available | Upstream | -433 |
| | | Upstream | -427 |
Matrix_153 | AP2 | Not available | Upstream | -435 |
| | | Upstream | -429 |
Matrix_155 | RAP2.6;ERF110;ABR1 | Not available | Upstream | -136 |
Matrix_156 | POC1 | Not available | Upstream | -427 |
Matrix_158 | AT1G03040;LRL1;UNE12;LRL2;LRL3 | Not available | Upstream | -434 |
| | | Upstream | -428 |
Matrix_183 | BES1 | A brassinosteroid transcriptional network revealed by genome-wide identification of BESI target genes in Arabidopsis thaliana | Upstream | -134 |
Matrix_186 | FHY3 | Not available | Upstream | -135 |
| | | Upstream | -115 |
Matrix_19 | PIF5 | Phytochrome interacting factors 4 and 5 control seedling growth in changing light conditions by directly controlling auxin signaling | Upstream | -428 |
Matrix_190 | ATERF1 | Not available | Upstream | -137 |
| | | Upstream | -136 |
Matrix_196 | TCP20;AT5G41030 | Not available | Upstream | -571 |
| | | Upstream | -567 |
| | | Upstream | -566 |
Matrix_200 | PIL5;AT4G28790;AT4G28800;AT4G28811;AT4G28815 | Not available | Upstream | -428 |
Matrix_214 | AP1 | Not available | Upstream | -436 |
Matrix_216 | TCP16 | Not available | Upstream | -569 |
Matrix_217 | BES1 | A brassinosteroid transcriptional network revealed by genome-wide identification of BESI target genes in Arabidopsis thaliana | Upstream | -437 |
Matrix_232 | TCP23 | Not available | Upstream | -570 |
| | | Upstream | -568 |
| | | Upstream | -567 |
Matrix_233 | MYC3 | Not available | Upstream | -433 |
| | | Upstream | -427 |
Matrix_234 | RAP2.3 | Not available | Upstream | -137 |
Matrix_243 | RAP2.12;RAP2.2 | Not available | Upstream | -136 |
Matrix_246 | ARR10 | Molecular structure of the GARP family of plant Myb-related DNA binding motifs of the Arabidopsis response regulators | Upstream | -292 |
Matrix_252 | RAP2.6 | Not available | Upstream | -137 |
Matrix_253 | ETT | Not available | Upstream | -588 |
Matrix_261 | ATERF-1 | Not available | Upstream | -137 |
Matrix_266 | TCP16 | Determinants of the DNA binding specificity of class I and class II TCP transcription factors | Upstream | -569 |
Matrix_269 | FHY3/FAR1 | Not available | Upstream | -256 |
Matrix_272 | DEAR4 | Not available | Upstream | -137 |
Matrix_278 | AtbZIP44 | Not available | Upstream | -832 |
Matrix_280 | TCP24;TCP1;BRC2;ATTCP18 | Not available | Upstream | -569 |
| | | Upstream | -568 |
Matrix_281 | TCP13 | Not available | Upstream | -569 |
Matrix_285 | DDF1 | Not available | Upstream | -587 |
Matrix_287 | ERF2 | Not available | Upstream | -137 |
Matrix_288 | RAP2.3 | Not available | Upstream | -138 |
Matrix_294 | MEE35 | Not available | Upstream | -569 |
Matrix_295 | ERF1 | Not available | Upstream | -137 |
Matrix_297 | TCP15 | Not available | Upstream | -570 |
| | | Upstream | -568 |
| | | Upstream | -567 |
Matrix_305 | PIF4 | Interaction between BZR1 and PIF4 integrates brassinosteroid and environmental responses | Upstream | -436 |
Matrix_320 | MYC4 | Not available | Upstream | -433 |
| | | Upstream | -427 |
Matrix_321 | HRD | Not available | Upstream | -137 |
Matrix_323 | BIM3 | Not available | Upstream | -428 |
Matrix_330 | MYC2;TT8 | Not available | Upstream | -428 |
Matrix_332 | SPT;ALC | Not available | Upstream | -434 |
| | | Upstream | -427 |
Matrix_334 | AT3G23230 | Not available | Upstream | -136 |
Matrix_343 | AT2G33710 | Not available | Upstream | -137 |
Matrix_344 | ATERF15;AT4G18450 | Not available | Upstream | -137 |
Matrix_345 | POC1 | Not available | Upstream | -432 |
Matrix_348 | AT5G51910 | Not available | Upstream | -569 |
| | | Upstream | -568 |
Matrix_355 | ERF10;ERF11 | Not available | Upstream | -138 |
Matrix_360 | ORA59 | Not available | Upstream | -137 |
Matrix_363 | RAP2.3 | Not available | Upstream | -138 |
Matrix_365 | AT1G10120;AT1G25330;CIB5;AT1G68920;AT3G23690;CIB1 | Not available | Upstream | -433 |
| | | Upstream | -427 |
Matrix_369 | AT2G18300 | Not available | Upstream | -436 |
| | | Upstream | -434 |
| | | Upstream | -430 |
Matrix_374 | AT5G07580;AT5G61590 | Not available | Upstream | -137 |
Matrix_377 | AT1G75490;DREB2C;AT2G40350;AT5G18450 | Not available | Upstream | -137 |
Matrix_378 | ATERF1 | Not available | Upstream | -137 |
Matrix_389 | ILR3 | Not available | Upstream | -428 |
Matrix_40 | TCP2 | Not available | Upstream | -569 |
Matrix_403 | BZR1 | Not available | Upstream | -430 |
Matrix_406 | ATERF-7 | Not available | Upstream | -139 |
Matrix_408 | GATA12 | Not available | Upstream | -292 |
Matrix_42 | AT2G45680 | Not available | Upstream | -569 |
| | | Upstream | -568 |
Matrix_426 | CRF1;CRF2 | Not available | Upstream | -136 |
Matrix_448 | ATERF6 | Not available | Upstream | -138 |
Matrix_449 | BIM2 | Not available | Upstream | -428 |
Matrix_45 | DRN | Not available | Upstream | -137 |
Matrix_462 | ATERF-8 | Not available | Upstream | -139 |
Matrix_465 | MYC4 | Not available | Upstream | -428 |
Matrix_473 | RRTF1 | Not available | Upstream | -137 |
Matrix_475 | AT5G64220 | Not available | Upstream | -135 |
| | | Upstream | -115 |
Matrix_476 | bHLH115;bHLH34 | Not available | Upstream | -433 |
| | | Upstream | -427 |
Matrix_480 | BES1 | Not available | Upstream | -435 |
| | | Upstream | -428 |
Matrix_484 | ATERF13 | Not available | Upstream | -137 |
Matrix_493 | AT1G22985;AT1G71130 | Not available | Upstream | -137 |
Matrix_506 | DRNL;ATERF-4 | Not available | Upstream | -136 |
Matrix_507 | TCP3 | Not available | Upstream | -570 |
| | | Upstream | -568 |
Matrix_517 | ERF12 | Not available | Upstream | -137 |
Matrix_53 | MYC3 | Not available | Upstream | -436 |
| | | Upstream | -432 |
| | | Upstream | -430 |
Matrix_55 | PIF3 | Not available | Upstream | -435 |
| | | Upstream | -429 |
Matrix_60 | AT1G01260;AT5G57150 | Not available | Upstream | -433 |
| | | Upstream | -427 |
Matrix_7 | PIF4 | Not available | Upstream | -426 |
Matrix_77 | PRR5 | Not available | Upstream | -435 |
| | | Upstream | -430 |
| | | Upstream | -135 |
Matrix_80 | BIM1 | Not available | Upstream | -433 |
| | | Upstream | -429 |
| | | Upstream | -132 |
Matrix_82 | TCP17 | Not available | Upstream | -569 |
Matrix_86 | CRF5;CRF6;CRF4 | Not available | Upstream | -136 |
Matrix_91 | CRF3 | Not available | Upstream | -137 |
Matrix_94 | TCP5 | Not available | Upstream | -569 |
Motif_121 | WRKY43;WRKY38;WRKY26 | Arabidopsis WRKY38 and WRKY62 transcription factors interact with histone deacetylase 19 in basal defense;Studies on DNA-binding selectivity of WRKY transcription factors lend structural clues into WRKY-domain function | Upstream | -388 |
Motif_139 | RHERPATEXPA7 | Right part of RHEs (Root Hair-specific cis-Elements) conserved among the Arabidopsis thaliana A7 (AtEXPA7) orthologous (and paralogous) genes from diverse angiosperm species with different hair distribution patterns | Upstream | -509 |
| | | Upstream | -431 |
| | | Upstream | -427 |
Motif_140 | DREB2A;DREB1A | Identification of cold-inducible downstream genes of the Arabidopsis DREB1A/CBF3 transcriptional factor using two microarray systems;Interaction between two cis-acting elements, ABRE and DRE, in ABA-dependent expression of Arabidopsis rd29A gene in response to dehydration and high-salinity stresses | Upstream | -41 |
Motif_145 | MYCATERD1 | MYC recognition sequence (from -466 to -461) necessary for expression of erd1 (early responsive to dehydration) in dehydrated Arabidopsis; NAC protein bound specifically to the CATGTG motif; NAC protein bound specifically to the CATGTG motif | Upstream | -84 |
Motif_155 | NODCON1GM | One of two putative nodulin consensus sequences; See also NODCON2GM; One of the consensus sequence motifs of organ-specific elements (OSE) characteristic of the promoters activated in infected cells of root nodules | Upstream | -413 |
Motif_179 | CACGTGMOTIF;BES1;PIF4;PIF5 | Phytochrome interacting factors 4 and 5 control seedling growth in changing light conditions by directly controlling auxin signaling;A brassinosteroid transcriptional network revealed by genome-wide identification of BESI target genes in Arabidopsis thaliana; CACGTG motif; G-box; Binding site of Arabidopsis GBF4; C. roseus G-box binding factor 1 (CrGBF1) and 1 (CrGBF2) can act as transcriptional repressors of the Str promoter via direct interaction with the G-box; Essential for expression of beta-phaseolin gene during embryogenesis in bean, tobacco, Arabidopsis; Tomato Pti4 (ERF) regulates defense-related gene expression via GCC box and non-GCC box cis-element (Myb1 (GTTAGTT) and G-box (CACGTG)); Isolation and characterization of a fourth Arabidopsis thaliana G-box-binding factor, which has similarities to Fos oncoprotein; Interaction between BZR1 and PIF4 integrates brassinosteroid and environmental responses | Upstream | -432 |
| | | Upstream | -426 |
Motif_189 | CMSRE1IBSPOA | CMSRE-1 (Carbohydrate Metabolite Signal Responsive Element 1) found in the promoter of sweet potato sporamin A gene | Upstream | -406 |
Motif_194 | EBOXBNNAPA | E-box of napA storage-protein gene of Brassica napus;This sequence is also known as RRE (R response element); MYC recognition site found in the promoters of the dehydration-responsive gene rd22 and many other genes in Arabidopsis; Binding site of ATMYC2 (previously known as rd22BP1); see E-box and MYCATRD22; MYC recognition sequence in CBF3 promoter; Binding site of ICE1 (inducer of CBF expression 1) that regulates the transcription of CBF/DREB1 genes in the cold in Arabidopsis; ICE1 | Upstream | -432 |
| | | Upstream | -426 |
| | | Upstream | -391 |
| | | Upstream | -84 |
Motif_216 | PYRIMIDINEBOXHVEPB1 | Pyrimidine box found in the barley EPB-1 (cysteine proteinase) gene promoter; Located between -120 to -113; Required for GA induction | Upstream | -177 |
Motif_218 | ABRERATCAL | ABRE-related sequence or Repeated sequence motifs identified in the upstream regions of 162 Ca(2+)-responsive upregulated genes; see also ABRE | Upstream | -433 |
| | | Upstream | -432 |
| | | Upstream | -427 |
| | | Upstream | -426 |
| | | Upstream | -132 |
| | | Upstream | -112 |
Motif_223 | LTRE1HVBLT49 | LTRE-1 (low-temperature-responsive element) in barley (H.v.) blt4.9 gene promoter; A new LTRE; A previously known LTRE is CCGAC | Upstream | -591 |
Motif_243 | TELOBOXATEEF1AA1 | telo-box (telomere motif) found in the Arabidopsis (A.t.) eEF1AA1 gene promoter; Conserved in all known plant eEF1A gene promoters; Found in the 5' region of numerous genes encoding components of the translational apparatus; Required for the activation of expression in root primordia; Acts co-operatively with tef-box; Binding site of AtPur alpha-1; Plant interstitial telomere mitifs participate in the control of gene expression in root meristems | Upstream | -520 |
Motif_244 | ABRE-like binding site motif | Not available | Upstream | -434 |
Motif_248 | L1-box | Arabidopsis DELLA and two HD-ZIP transcription factors regulate GA signaling in the epidermis through the L1 box cis-element | Upstream | -514 |
Motif_249 | DPBF1&2 binding site motif | A novel class of bZIP transcription factors, DPBF-1 and 2 (Dc3 promoter-binding factor-1 and 2) binding core sequence; Found in the carrot Dc3 gene promoter; Dc3 expression is normally embryo-specific, and also can be induced by ABA; The Arabidopsis abscisic acid response gene ABI5 encodes a bZIP transcription factor; abi5 mutant have a pleiotropic defects in ABA response; ABI5 regulates a subset of late embryogenesis-abundant genes; GIA1 (growth-insensitivity to ABA) is identical to ABI5; Isolation of a novel class of bZIP transcription factors that interact with ABA-responsive and embryo-specification elements in the Dc3 promoter using a modified yeast one-hybrid system | Upstream | -84 |
Motif_254 | MYB46;MYB83 | MYB46 and MYB83 bind to the SMRE sites and directly activate a suite of transcription factors and secondary wall biosynthetic genes | Upstream | -390 |
Motif_270 | ELRECOREPCRP1 | ElRE (Elicitor Responsive Element) core of parsley PR1 genes; consensus sequence of elements W1 and W2 of parsley PR1-1 and PR1-2 promoters; Box W1 and W2 are the binding site of WRKY1 and WRKY2, respectively; ERE; WA box; One of the W boxes found in the Parsley WRKY1 gene promoter; Required for elicitor responsiveness; WC box WB box and WC box constitute a palindrome; WRKY1 protein binding site; W-box found in thioredoxin h5 gene in Arabidopsis | Upstream | -386 |
Motif_297 | Bellringer/replumless/pennywise BS1 IN AG | Repression of AGAMOUS by BELLRINGER in Floral and Inflorescence Meristems | Upstream | -1691 |
Motif_313 | ERF1 BS in AtCHI-B | Core of GCC-box found in many pathogen-responsive genes such as PDF1.2, Thi2.1, and PR4; Has been shown to function as ethylene-responsive element; Appears to play important roles in regulating jasmonate-responsive gene expression; Tomato Pti4 (ERF) regulates defence-related gene expression via GCC box and non-GCC box cis elements (Myb1 (GTTAGTT) and G-box(CACGTG)); Nuclear events in ethylene signaling: a transcriptional cascade mediated by ETHYLENE-INSENSITIVE3 and ETHYLENE-RESPONSE-FACTOR1;Molecular responses to dehydration and low temperature | Upstream | -136 |
Motif_318 | CGCGBOXAT | CGCG box recognized by AtSR1-6 (Arabidopsis thaliana signal-responsive genes); Multiple CGCG elements are found in promoters of many genes; Ca2+/calmodulin binds to all AtSRs | Upstream | -132 |
| | | Upstream | -112 |
Motif_339 | ABRE-like binding site motif | Molecular responses to dehydration and low temperature | Upstream | -432 |
| | | Upstream | -426 |
Motif_346 | SND1;VND6;VND7;NST1;NST2 | Global analysis of direct targets of secondary wall NAC master switches in Arabidopsis | Upstream | -408 |
Motif_353 | HEXAMERATH4 | hexamer motif of Arabidopsis thaliana histone H4 promoter;Identification of cis-elements regulating the expression of an Arabidopsis histone H4 gene | Upstream | -325 |
| | | Upstream | -50 |
Motif_358 | UP2ATMSD | Up2 motif found in 193 of the 1184 up-regulated genes after main stem decapitation in Arabidopsis | Upstream | -520 |
Motif_371 | DRE-like promoter motif | The Expression Profile Matrix of Arabidopsis Transcription Factor Genes Suggests Their Putative Functions in Response to Environmental Stresses | Upstream | -39 |
Motif_383 | UPRE-III(bZIP60) | The plant-specific transcription factor NAC103 is induced by bZIP60 through a new cis-regulatory element to modulate the unfolded protein response in Arabidopsis | Upstream | -444 |
Motif_392 | PALBOXAPC | Box A; Consensus; One of three putative cis-acting elements (boxes P, A, and L) of phenylalanine ammonia-lyase (PAL; EC 4.3.1.5) genes in parsley (P.c.); None of these elements (boxes P, A, and L) alone, or the promoter region containing all of them together, conferred elicitor or light responsiveness. These elements appear to be necessary but not sufficient for elicitor- or light-mediated PAL gene activation; See also Box P, Box L | Upstream | -406 |
Motif_411 | PRECONSCRHSP70A | Consensus sequence of PRE (plastid response element) in the promoters of HSP70A in Chlamydomonas; Involved in induction of HSP70A gene by both MgProto and light | Upstream | -57 |
Motif_447 | AtMYC2 BS in RD22;PIF4 | Binding site for MYC (rd22BP1) in Arabidopsis dehydration-resposive gene, rd22; MYC binding site in rd22 gene of Arabidopsis thaliana; ABA-induction; Located at ca. -200 of rd22 gene; Also MYB at ca. -141 of rd22 gene; See also MYBATRD22; Role of Arabidopsis MYC and MYB homologs in drought- and abscisic acid-regulated gene expression. Interaction between BZR1 and PIF4 integrates brassinosteroid and environmental responses | Upstream | -84 |
Motif_448 | IRO2OS | OsIRO2-binding core sequence; G-box plus G; Transcription factor OsIRO2 is induced exclusively by Fe deficiency | Upstream | -433 |
| | | Upstream | -426 |
Motif_454 | DRECRTCOREAT | Core motif of DRE/CRT (dehydration-responsive element/C-repeat) cis-acting element found in many genes in Arabidopsis and in rice; Os DREB1A bound to GCCGAC more preferentially than to ACCGAC whereas At DREB1A bound to both GCCGAC and ACCGAC efficiently; Maize ZmDREB1A bound to DRE; HaDREB2 in Helianthus annuus (sunflower) | Upstream | -38 |
Motif_469 | QELEMENTZMZM13 | Q(quantitative)-element in maize ZM13 gene promoter; Found at -107 to -102; Involved in expression enhancing activity; ZM13 is a maize homolog of tomato LAT52 gene; ZM13 is a pollen-specific maize gene | Upstream | -395 |
Motif_48 | BES1 | A brassinosteroid transcriptional network revealed by genome-wide identification of BESI target genes in Arabidopsis thaliana | Upstream | -667 |
Motif_503 | EECCRCAH1 | EEC; Consensus motif of the two enhancer elements, EE-1 and EE-2, both found in the promoter region of the Chlamydomonas Cah1 (encoding a periplasmic carbonic anhydrase); Binding site of Myb transcription factor LCR1 | Upstream | -104 |
Motif_517 | LEAFYATAG | Target sequence of LEAFY in the intron of AGAMOUS gene in Arabidopsis | Upstream | -65 |
Motif_525 | CRTDREHVCBF2 | Preferred sequence for AP2 transcriptional activator HvCBF2 of barley; Core CRT/DRE motif; HvCBF2 bound to a (G/a)(T/c)CGAC core motif; DNA binding is regulated by temperature | Upstream | -586 |
Motif_54 | LTREATLTI78 | Putative low temperature responsive element (LTRE); Found in Arabidopsis thaliana low-temperature-induced (lti) genes, lti78 and lti65; Repeated four times in lti78 which is also known as cor78 and rd29A; Found also in barley low temperature responsive genes, blt4.2, blt4.6, blt4.9 (lipid transfer genes); cold inducible; See LTRECORE; Also present in rab18, kin1, and kin2; Differential expression of two related, low-temperature-induced genes in Arabidopsis thaliana | Upstream | -39 |
Motif_549 | TBF1 | The HSF-like transcription factor TBF1 is a major molecular switch for plant growth-to-defense transition | Upstream | -253 |
Motif_580 | L1BOXATPDF1 | L1 box found in promoter of Arabidopsis thaliana PROTODERMAL FACTOR1 (PDF1) gene; Located between -134 and -127; Involved in L1 layer-specific expression; L1-specific homeodomain protein ATML can bind to the L1 box; Y=C/T; A cotton fiber gene, RD22-like 1 (RDL1), contains a homeodomain binding L1 box and a MYB binding motif ; HDZip IV; Identification of a cis-regulatory element for L1 layer-specific gene expression, which is targeted by an L1-specific homeodomain protein | Upstream | -514 |
Motif_584 | UPRE-III(bZIP60) | The plant-specific transcription factor NAC103 is induced by bZIP60 through a new cis-regulatory element to modulate the unfolded protein response in Arabidopsis | Upstream | -444 |
Motif_591 | CBFHV | Binding site of barley CBF1, and also of barley CBF2; CBF = C-repeat (CRT) binding factors; CBFs are also known as dehydration-responsive element (DRE) binding proteins (DREBs) | Upstream | -586 |
| | | Upstream | -327 |
| | | Upstream | -38 |
Motif_603 | SITEIIATCYTC | Site II element found in the promoter regions of cytochrome genes (Cytc-1, Cytc-2) in Arabidopsis; Located between -147 and -156 from the translational starts sites;Overrepresented in the promoters of nuclear genes encoding components of the oxidative phosphorylation (OxPhos) machinery from both Arabidopsis and rice | Upstream | -568 |
| | | Upstream | -496 |
Motif_606 | NAPINMOTIFBN | Sequence found in 5' upstream region (-6, -95, -188) of napin (2S albumin) gene in Brassica napus; Interact with a protein present in crude nuclear extracts from developing B. napus seeds | Upstream | -83 |
Motif_630 | WBOXNTCHN48 | W box identified in the region between -125 and -69 of a tobacco class I basic chitinase gene CHN48; NtWRKY1, NtWRKY2 and NtWRKY4 bound to W box; NtWRKYs possibly involved in elicitor-respsonsive transcription of defense genes in tobacco | Upstream | -237 |
Motif_643 | DRE2COREZMRAB17 | DRE2 core found in maize rab17 gene promoter; DBF1 and DBF2 bound to DRE2; rab17 is expressed during late embryogenesis, and is induced by ABA | Upstream | -38 |
Motif_658 | GT1CONSENSUS | Consensus GT-1 binding site in many light-regulated genes, e.g., RBCS from many species, PHYA from oat and rice, spinach RCA and PETA, and bean CHS15; GT-1 can stabilize the TFIIA-TBP-DNA (TATA box) complex; The activation mechanism of GT-1 may be achieved through direct interaction between TFIIA and GT-1; Binding of GT-1-like factors to the PR-1a promoter influences the level of SA-inducible gene expression | Upstream | -301 |
| | | Upstream | -176 |
| | | Upstream | -175 |
| | | Upstream | -59 |
Motif_682 | GT1GMSCAM4 | GT-1 motif found in the promoter of soybean CaM isoform, SCaM-4; Plays a role in pathogen- and salt-induced SCaM-4 gene expression | Upstream | -301 |
| | | Upstream | -176 |
Motif_83 | CIACADIANLELHC | Region necessary for circadian expression of tomato Lhc gene | Upstream | -492 |
Motif_94 | UP1ATMSD | Up1 motif found in 162 of the 1184 up-regulated genes after main stem decapitation in Arabidopsis | Upstream | -496 |
Motif_98 | SEF3MOTIFGM | SEF3 binding site; Soybean consensus sequence found in the 5' upstream region of beta-conglycinin (7S globulin) gene; AACCCA(-27bp-)AACCCA; SEF=soybean embryo factor; SEF2; SEF3; SEF4 | Upstream | -422 |