Matrix_101 | ERF5 | Not available | Upstream | -145 |
| | | Upstream | -146 |
Matrix_104 | PI | Not available | Upstream | -426 |
| | | Upstream | -427 |
Matrix_105 | SPL14 | Not available | Upstream | -13 |
| | | Upstream | -14 |
Matrix_109 | GBF3 | Not available | Upstream | -102 |
| | | Upstream | -426 |
| | | Upstream | -427 |
| | | Upstream | -428 |
| | | Upstream | -429 |
Matrix_110 | ATABI4;AT3G57600 | Not available | Upstream | -145 |
| | | Upstream | -146 |
| | | Upstream | -158 |
Matrix_113 | ABI5 | Not available | Upstream | -426 |
| | | Upstream | -427 |
| | | Upstream | -428 |
| | | Upstream | -429 |
Matrix_117 | ANT | Not available | Upstream | -440 |
Matrix_118 | PIF3_2 | Direct targeting of light signals to a promoter element-bound transcription factor | Upstream | -100 |
| | | Upstream | -423 |
| | | Upstream | -424 |
Matrix_120 | BEE2 | Not available | Upstream | -427 |
| | | Upstream | -428 |
Matrix_122 | ABF1;AREB2 | Not available | Upstream | -427 |
| | | Upstream | -428 |
Matrix_129 | ABF1 | Not available | Upstream | -427 |
| | | Upstream | -428 |
Matrix_134 | ABF1 | Not available | Upstream | -427 |
| | | Upstream | -428 |
Matrix_137 | SPL1;SPL12 | Not available | Upstream | -18 |
Matrix_138 | RRTF1 | Not available | Upstream | -147 |
Matrix_14 | ZCW32;AT5G62610 | Not available | Upstream | -104 |
Matrix_142 | ZFP8 | Not available | Upstream | -48 |
Matrix_143 | GATA14;GATA6;GATA5 | Not available | Upstream | -389 |
| | | Upstream | -390 |
| | | Upstream | -391 |
| | | Upstream | -392 |
| | | Upstream | -440 |
| | | Upstream | -441 |
| | | Upstream | -442 |
| | | Upstream | -443 |
Matrix_145 | GBF4;AT5G44080 | Not available | Upstream | -428 |
| | | Upstream | -429 |
Matrix_146 | ORA47 | Not available | Upstream | -145 |
| | | Upstream | -146 |
Matrix_147 | ERF3;AT1G80580 | Not available | Upstream | -147 |
Matrix_151 | ASIL1 | Not available | Upstream | -42 |
| | | Upstream | -43 |
| | | Upstream | -147 |
| | | Upstream | -150 |
Matrix_155 | RAP2.6;ERF110;ABR1 | Not available | Upstream | -146 |
| | | Upstream | -147 |
Matrix_156 | POC1 | Not available | Upstream | -102 |
| | | Upstream | -426 |
| | | Upstream | -427 |
Matrix_161 | MYBC1;AT3G10760;LUX;AT5G05090;AT5G59570 | Not available | Upstream | -441 |
Matrix_169 | E2F1 | Not available | Upstream | -144 |
| | | Upstream | -145 |
Matrix_180 | SPL1 | Not available | Upstream | -18 |
Matrix_183 | BES1 | A brassinosteroid transcriptional network revealed by genome-wide identification of BESI target genes in Arabidopsis thaliana | Upstream | -121 |
| | | Upstream | -122 |
| | | Upstream | -141 |
| | | Upstream | -142 |
Matrix_186 | FHY3 | Not available | Upstream | -121 |
| | | Upstream | -122 |
| | | Upstream | -141 |
| | | Upstream | -142 |
Matrix_188 | SPL4 | Not available | Upstream | -17 |
| | | Upstream | -20 |
Matrix_190 | ATERF1 | Not available | Upstream | -144 |
| | | Upstream | -145 |
| | | Upstream | -146 |
Matrix_192 | FHY3/FAR1 | Not available | Upstream | -424 |
| | | Upstream | -425 |
| | | Upstream | -428 |
| | | Upstream | -429 |
Matrix_194 | HYH;HY5 | Not available | Upstream | -424 |
| | | Upstream | -425 |
Matrix_195 | GATA2;GATA4 | Not available | Upstream | -390 |
| | | Upstream | -441 |
Matrix_199 | AT1G69170;SPL9;SPL15;SPL13A;SPL13B | Not available | Upstream | -18 |
| | | Upstream | -19 |
Matrix_200 | PIL5;AT4G28790;AT4G28800;AT4G28811;AT4G28815 | Not available | Upstream | -427 |
| | | Upstream | -428 |
Matrix_203 | GATA9;GATA12 | Not available | Upstream | -389 |
| | | Upstream | -390 |
| | | Upstream | -391 |
Matrix_21 | HSFC1 | Not available | Upstream | -297 |
Matrix_214 | AP1 | Not available | Upstream | -425 |
| | | Upstream | -426 |
Matrix_217 | BES1 | A brassinosteroid transcriptional network revealed by genome-wide identification of BESI target genes in Arabidopsis thaliana | Upstream | -424 |
| | | Upstream | -425 |
| | | Upstream | -428 |
| | | Upstream | -429 |
Matrix_221 | SPL7 | Not available | Upstream | -17 |
Matrix_226 | GATA1 | Not available | Upstream | -390 |
| | | Upstream | -391 |
Matrix_234 | RAP2.3 | Not available | Upstream | -145 |
| | | Upstream | -146 |
Matrix_243 | RAP2.12;RAP2.2 | Not available | Upstream | -146 |
| | | Upstream | -147 |
Matrix_246 | ARR10 | Molecular structure of the GARP family of plant Myb-related DNA binding motifs of the Arabidopsis response regulators | Upstream | -281 |
| | | Upstream | -282 |
Matrix_247 | PIF3 | Not available | Upstream | -103 |
| | | Upstream | -427 |
| | | Upstream | -428 |
Matrix_252 | RAP2.6 | Not available | Upstream | -145 |
| | | Upstream | -146 |
Matrix_256 | IXR11;KNAT5;KNAT4;KNAT3 | Not available | Upstream | -370 |
Matrix_260 | CAMTA3 | Not available | Upstream | -103 |
Matrix_261 | ATERF-1 | Not available | Upstream | -146 |
| | | Upstream | -147 |
Matrix_264 | ATAREB1 | Not available | Upstream | -424 |
| | | Upstream | -425 |
| | | Upstream | -427 |
| | | Upstream | -428 |
Matrix_272 | DEAR4 | Not available | Upstream | -145 |
| | | Upstream | -146 |
Matrix_286 | GATA7 | Not available | Upstream | -390 |
| | | Upstream | -391 |
Matrix_287 | ERF2 | Not available | Upstream | -145 |
Matrix_288 | RAP2.3 | Not available | Upstream | -147 |
Matrix_295 | ERF1 | Not available | Upstream | -147 |
Matrix_296 | GBF2 | Not available | Upstream | -103 |
| | | Upstream | -427 |
| | | Upstream | -428 |
| | | Upstream | -429 |
Matrix_300 | bZIP68;bZIP16 | Not available | Upstream | -103 |
| | | Upstream | -427 |
| | | Upstream | -428 |
| | | Upstream | -429 |
Matrix_301 | PIL5 | Not available | Upstream | -428 |
| | | Upstream | -429 |
Matrix_305 | PIF4 | Interaction between BZR1 and PIF4 integrates brassinosteroid and environmental responses | Upstream | -149 |
| | | Upstream | -288 |
| | | Upstream | -289 |
Matrix_307 | RGL2;RGL3 | Not available | Upstream | -17 |
Matrix_31 | SPL1 | Not available | Upstream | -17 |
| | | Upstream | -19 |
Matrix_313 | ATMYB65;MYB33 | Not available | Upstream | -402 |
Matrix_321 | HRD | Not available | Upstream | -146 |
Matrix_326 | AT5G07310;Rap2.6L;AT5G61890 | Not available | Upstream | -147 |
Matrix_328 | AT1G76580 | Not available | Upstream | -18 |
Matrix_33 | SPL11;SPL10;SPL2 | Not available | Upstream | -17 |
Matrix_331 | GBF1 | Not available | Upstream | -426 |
| | | Upstream | -427 |
| | | Upstream | -428 |
| | | Upstream | -429 |
Matrix_332 | SPT;ALC | Not available | Upstream | -104 |
| | | Upstream | -427 |
| | | Upstream | -428 |
Matrix_333 | GATA3 | Not available | Upstream | -391 |
| | | Upstream | -392 |
Matrix_334 | AT3G23230 | Not available | Upstream | -146 |
Matrix_335 | HSFB2A | Not available | Upstream | -302 |
Matrix_338 | AP2 | Not available | Upstream | -424 |
| | | Upstream | -425 |
Matrix_339 | bHLH104 | Not available | Upstream | -427 |
Matrix_342 | SPL14 | Identification of a Consensus DNA-Binding Site for the Arabidopsis thaliana SBP Domain Transcription Factor, AtSPL14, and Binding Kinetics by Surface Plasmon Resonance | Upstream | -13 |
| | | Upstream | -14 |
Matrix_343 | AT2G33710 | Not available | Upstream | -145 |
| | | Upstream | -146 |
Matrix_344 | ATERF15;AT4G18450 | Not available | Upstream | -147 |
Matrix_345 | POC1 | Not available | Upstream | -100 |
Matrix_355 | ERF10;ERF11 | Not available | Upstream | -147 |
Matrix_356 | PRR5 | Not available | Upstream | -420 |
| | | Upstream | -421 |
| | | Upstream | -424 |
| | | Upstream | -425 |
Matrix_360 | ORA59 | Not available | Upstream | -147 |
Matrix_363 | RAP2.3 | Not available | Upstream | -147 |
Matrix_374 | AT5G07580;AT5G61590 | Not available | Upstream | -146 |
Matrix_377 | AT1G75490;DREB2C;AT2G40350;AT5G18450 | Not available | Upstream | -146 |
Matrix_378 | ATERF1 | Not available | Upstream | -145 |
| | | Upstream | -146 |
Matrix_38 | SPL14 | Not available | Upstream | -18 |
Matrix_389 | ILR3 | Not available | Upstream | -103 |
| | | Upstream | -427 |
| | | Upstream | -428 |
Matrix_403 | BZR1 | Not available | Upstream | -101 |
| | | Upstream | -139 |
| | | Upstream | -140 |
| | | Upstream | -425 |
| | | Upstream | -426 |
Matrix_408 | GATA12 | Not available | Upstream | -390 |
| | | Upstream | -391 |
Matrix_426 | CRF1;CRF2 | Not available | Upstream | -146 |
Matrix_438 | AtbZIP63 | Not available | Upstream | -427 |
| | | Upstream | -428 |
Matrix_443 | AGL15 | Not available | Upstream | -425 |
| | | Upstream | -426 |
Matrix_448 | ATERF6 | Not available | Upstream | -147 |
| | | Upstream | -150 |
Matrix_45 | DRN | Not available | Upstream | -147 |
Matrix_450 | SPL7 | Not available | Upstream | -17 |
| | | Upstream | -19 |
Matrix_452 | MYB46 | Not available | Downstream | 2044 |
Matrix_462 | ATERF-8 | Not available | Upstream | -148 |
Matrix_466 | PRR5 | Not available | Upstream | -424 |
Matrix_473 | RRTF1 | Not available | Upstream | -145 |
| | | Upstream | -146 |
Matrix_475 | AT5G64220 | Not available | Upstream | -124 |
| | | Upstream | -125 |
| | | Upstream | -144 |
| | | Upstream | -145 |
Matrix_480 | BES1 | Not available | Upstream | -426 |
| | | Upstream | -427 |
Matrix_484 | ATERF13 | Not available | Upstream | -147 |
Matrix_488 | ABF1 | Not available | Upstream | -141 |
| | | Upstream | -390 |
| | | Upstream | -391 |
| | | Upstream | -419 |
| | | Upstream | -420 |
| | | Upstream | -426 |
| | | Upstream | -427 |
Matrix_49 | FHY3/FAR1 | Not available | Upstream | -118 |
Matrix_490 | AtMYB77;ATMYB44 | Not available | Upstream | -404 |
Matrix_493 | AT1G22985;AT1G71130 | Not available | Upstream | -146 |
Matrix_5 | AT5G51190;ERF104 | Not available | Upstream | -147 |
Matrix_505 | GATA8 | Not available | Upstream | -391 |
| | | Upstream | -392 |
| | | Upstream | -442 |
| | | Upstream | -443 |
Matrix_506 | DRNL;ATERF-4 | Not available | Upstream | -146 |
| | | Upstream | -147 |
Matrix_517 | ERF12 | Not available | Upstream | -147 |
Matrix_53 | MYC3 | Not available | Upstream | -143 |
| | | Upstream | -144 |
Matrix_55 | PIF3 | Not available | Upstream | -426 |
| | | Upstream | -427 |
Matrix_60 | AT1G01260;AT5G57150 | Not available | Upstream | -428 |
Matrix_63 | ARR10 | Not available | Upstream | -443 |
Matrix_65 | POC1;PIL1 | Not available | Upstream | -428 |
Matrix_68 | AtMYB77 | More than 80 R2R3-MYB regulatory genes in the genome of Arabidopsis thaliana. Plant J 14: 273-84 | Upstream | -400 |
Matrix_7 | PIF4 | Not available | Upstream | -427 |
| | | Upstream | -428 |
| | | Upstream | -429 |
| | | Upstream | -430 |
Matrix_77 | PRR5 | Not available | Upstream | -102 |
| | | Upstream | -120 |
| | | Upstream | -121 |
| | | Upstream | -140 |
| | | Upstream | -141 |
| | | Upstream | -425 |
| | | Upstream | -426 |
| | | Upstream | -427 |
Matrix_80 | BIM1 | Not available | Upstream | -120 |
| | | Upstream | -121 |
| | | Upstream | -140 |
| | | Upstream | -141 |
| | | Upstream | -428 |
| | | Upstream | -429 |
Matrix_85 | SPL5 | Not available | Upstream | -18 |
Matrix_86 | CRF5;CRF6;CRF4 | Not available | Upstream | -146 |
| | | Upstream | -147 |
Matrix_91 | CRF3 | Not available | Upstream | -146 |
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 | -495 |
| | | Upstream | -517 |
Motif_150 | RBCSCONSENSUS | rbcS general consensus sequence; AATCCAA or AATCCAAC | Upstream | -480 |
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 | -429 |
Motif_182 | MYB2CONSENSUSAT | MYB recognition site found in the promoters of the dehydration-responsive gene rd22 and many other genes in Arabidopsis; see MYB2 and MYBATRD22 | Upstream | -129 |
| | | Upstream | -321 |
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 | -429 |
Motif_200 | GBOXLERBCS | G box; Conserved sequence upstream of light-regulated genes; Sequence found in the promoter region of rbcS of tomato and Arabidopsis; Binding with GBF | Upstream | -427 |
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 | -104 |
| | | Upstream | -123 |
| | | Upstream | -143 |
| | | Upstream | -428 |
| | | Upstream | -429 |
| | | Upstream | -721 |
| | | Upstream | -722 |
Motif_221 | MYBCORE | Binding site for all animal MYB and at least two plant MYB proteins ATMYB1 and ATMYB2, both isolated from Arabidopsis; ATMYB2 is involved in regulation of genes that are responsive to water stress in Arabidopsis; A petunia MYB protein (MYB.Ph3) is involved in regulation of flavonoid biosynthesis | Upstream | -129 |
| | | Upstream | -321 |
| | | Upstream | -406 |
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 | -377 |
Motif_244 | ABRE-like binding site motif | Not available | Upstream | -427 |
| | | Upstream | -429 |
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 | -429 |
Motif_291 | ABFs binding site motif | Binding site of trans-acting factor EMBP-1; wheat Em gene;Binding site of ABFs; ABFs (ABRE binding factors) were isolated from Arabidopsis by a yeast one-hybrid screening system; Expression ABFs is induced by ABA and various stress treatment; ABFs belongs to a distinct subfamily of bZIP proteins; Involved in ABA-mediated stress-signaling pathway;A plant leucine zipper protein that recognizes an abscisic acid response element | Upstream | -427 |
Motif_309 | GATA promoter motif | Arabidopsis thaliana GATA factors: organisation, expression and DNA-binding characteristics | Upstream | -314 |
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 | -148 |
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 | -105 |
| | | Upstream | -124 |
| | | Upstream | -144 |
| | | Upstream | -722 |
Motif_336 | MYBMOUSE | Binding site for mouse c-myb protein | Upstream | -129 |
| | | Upstream | -321 |
Motif_339 | ABRE-like binding site motif | Molecular responses to dehydration and low temperature | Upstream | -429 |
Motif_346 | SND1;VND6;VND7;NST1;NST2 | Global analysis of direct targets of secondary wall NAC master switches in Arabidopsis | Upstream | -392 |
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 | -280 |
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 | -403 |
Motif_448 | IRO2OS | OsIRO2-binding core sequence; G-box plus G; Transcription factor OsIRO2 is induced exclusively by Fe deficiency | Upstream | -428 |
Motif_48 | BES1 | A brassinosteroid transcriptional network revealed by genome-wide identification of BESI target genes in Arabidopsis thaliana | Upstream | -1705 |
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 | -413 |
Motif_542 | ABI5;AtMYC2;HY5 | A basic helix-loop-helix transcription factor in Arabidopsis, MYC2, acts as a repressor of blue light-mediated photomorphogenic growth. Arabidopsis bZIP protein HY5 directly interacts with light-responsive promoters in mediating light control of gene expression. The homologous ABI5 and EEL transcription factors function antagonistically to fine-tune gene expression during late embryogenesis | Upstream | -427 |
Motif_558 | BOXIIPCCHS | Core of Box II/G box found in the parsley chs genes; Essential for light regulation | Upstream | -427 |
Motif_561 | GATA-2;GATA-4;GATA-3;GATA-1 | Arabidopsis thaliana GATA factors: organisation, expression and DNA-binding characteristics | Upstream | -254 |
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 | -280 |
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 | -434 |
Motif_609 | AP2 | The floral homeotic protein APETALA2 recognizes and acts through an AT-rich sequence element | Upstream | -112 |
Motif_627 | ACGTABREMOTIFA2OSEM | Experimentally determined sequence requirement of ACGT-core of motif A in ABRE of the rice gene, OSEM; DRE and ABRE are interdependent in the ABA-responsive expression of the rd29A in Arabidopsis | Upstream | -427 |
| | | Upstream | -430 |
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 | -83 |
| | | Upstream | -384 |
Motif_638 | ABRE binding site motif | Not available | Upstream | -427 |
Motif_641 | LRENPCABE | LRE; A positive light regulatory element in tobacco CAB (cab-E) gene; Located at -241 | Upstream | -426 |
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 | -134 |
| | | Upstream | -313 |
| | | Upstream | -414 |
Motif_672 | AP2 | The floral homeotic protein APETALA2 recognizes and acts through an AT-rich sequence element | Upstream | -112 |
Motif_688 | AMMORESIVDCRNIA1 | Motif (IVD) found in the Chlamydomonas Nia1 gene promoter; Located between -51 and -42; Involved in Nia1 transcription repression | Upstream | -51 |
| | | Upstream | -220 |
Motif_72 | GADOWNAT | Sequence present in 24 genes in the GA-down regulated d1 cluster (106 genes) found in Arabidopsis seed germination; This motif is similar to ABRE | Upstream | -430 |
Motif_83 | CIACADIANLELHC | Region necessary for circadian expression of tomato Lhc gene | Upstream | -413 |
Motif_92 | ABREATRD22 | ABRE (ABA responsive element) in Arabidopsis dehydration-responsive gene rd22 | Upstream | -426 |