Matrix_104 | PI | Not available | Upstream | -245 |
Matrix_106 | AT5G47390 | Not available | Upstream | -292 |
Matrix_109 | GBF3 | Not available | Upstream | -245 |
| | | Upstream | -246 |
| | | Upstream | -247 |
Matrix_113 | ABI5 | Not available | Upstream | -245 |
| | | Upstream | -246 |
| | | Upstream | -247 |
Matrix_119 | RRTF1 | Not available | Upstream | -286 |
Matrix_120 | BEE2 | Not available | Upstream | -245 |
| | | Upstream | -246 |
Matrix_122 | ABF1;AREB2 | Not available | Upstream | -245 |
| | | Upstream | -246 |
Matrix_129 | ABF1 | Not available | Upstream | -245 |
| | | Upstream | -246 |
Matrix_134 | ABF1 | Not available | Upstream | -246 |
| | | Upstream | -247 |
Matrix_138 | RRTF1 | Not available | Upstream | -286 |
Matrix_145 | GBF4;AT5G44080 | Not available | Upstream | -246 |
| | | Upstream | -247 |
Matrix_15 | PIF3_1 | Direct targeting of light signals to a promoter element-bound transcription factor | Upstream | -242 |
Matrix_156 | POC1 | Not available | Upstream | -246 |
| | | Upstream | -247 |
Matrix_192 | FHY3/FAR1 | Not available | Upstream | -243 |
| | | Upstream | -246 |
| | | Upstream | -247 |
Matrix_194 | HYH;HY5 | Not available | Upstream | -243 |
Matrix_200 | PIL5;AT4G28790;AT4G28800;AT4G28811;AT4G28815 | Not available | Upstream | -245 |
| | | Upstream | -246 |
Matrix_201 | AT1G74840 | Not available | Upstream | -291 |
Matrix_206 | CUC1;ANAC100 | Not available | Upstream | -249 |
Matrix_214 | AP1 | Not available | Upstream | -244 |
Matrix_217 | BES1 | A brassinosteroid transcriptional network revealed by genome-wide identification of BESI target genes in Arabidopsis thaliana | Upstream | -246 |
| | | Upstream | -247 |
Matrix_24 | POC1 | Not available | Upstream | -242 |
Matrix_247 | PIF3 | Not available | Upstream | -245 |
| | | Upstream | -246 |
Matrix_257 | NAC050;ANAC051;anac057;NAC2 | Not available | Upstream | -249 |
Matrix_264 | ATAREB1 | Not available | Upstream | -243 |
| | | Upstream | -245 |
| | | Upstream | -246 |
Matrix_268 | EMB2749;VND5;SMB;VND1;ANAC076;NAC101;ANAC105 | Not available | Upstream | -251 |
Matrix_271 | AT3G16350 | Not available | Upstream | -292 |
Matrix_277 | RAP2.6 | Not available | Upstream | -286 |
Matrix_296 | GBF2 | Not available | Upstream | -245 |
| | | Upstream | -246 |
| | | Upstream | -247 |
Matrix_298 | RAV1 | Not available | Upstream | -281 |
Matrix_300 | bZIP68;bZIP16 | Not available | Upstream | -245 |
| | | Upstream | -246 |
| | | Upstream | -247 |
Matrix_301 | PIL5 | Not available | Upstream | -241 |
| | | Upstream | -246 |
| | | Upstream | -247 |
Matrix_322 | NST3;ANAC015;BRN2 | Not available | Upstream | -250 |
Matrix_326 | AT5G07310;Rap2.6L;AT5G61890 | Not available | Upstream | -286 |
Matrix_331 | GBF1 | Not available | Upstream | -245 |
| | | Upstream | -246 |
| | | Upstream | -247 |
Matrix_332 | SPT;ALC | Not available | Upstream | -246 |
| | | Upstream | -247 |
Matrix_336 | AT5G08520 | Not available | Upstream | -293 |
Matrix_338 | AP2 | Not available | Upstream | -243 |
Matrix_339 | bHLH104 | Not available | Upstream | -245 |
| | | Upstream | -246 |
Matrix_343 | AT2G33710 | Not available | Upstream | -287 |
Matrix_355 | ERF10;ERF11 | Not available | Upstream | -286 |
Matrix_356 | PRR5 | Not available | Upstream | -239 |
| | | Upstream | -243 |
Matrix_359 | FLC | Not available | Upstream | -244 |
Matrix_363 | RAP2.3 | Not available | Upstream | -286 |
Matrix_389 | ILR3 | Not available | Upstream | -245 |
| | | Upstream | -246 |
Matrix_403 | BZR1 | Not available | Upstream | -244 |
Matrix_41 | anac058 | Not available | Upstream | -249 |
Matrix_413 | RAV1 | Not available | Upstream | -281 |
Matrix_420 | ANAC58 | Not available | Upstream | -250 |
Matrix_426 | CRF1;CRF2 | Not available | Upstream | -288 |
Matrix_44 | CUC3;anac046;NAC3;ANAC087;ATNAC6;CUC2 | Not available | Upstream | -250 |
Matrix_443 | AGL15 | Not available | Upstream | -244 |
Matrix_473 | RRTF1 | Not available | Upstream | -287 |
Matrix_480 | BES1 | Not available | Upstream | -245 |
| | | Upstream | -246 |
Matrix_488 | ABF1 | Not available | Upstream | -238 |
| | | Upstream | -245 |
| | | Upstream | -250 |
Matrix_489 | RAV1 | Not available | Upstream | -283 |
Matrix_493 | AT1G22985;AT1G71130 | Not available | Upstream | -287 |
Matrix_506 | DRNL;ATERF-4 | Not available | Upstream | -288 |
Matrix_53 | MYC3 | Not available | Upstream | -247 |
| | | Upstream | -248 |
Matrix_55 | PIF3 | Not available | Upstream | -245 |
Matrix_57 | WIN1;SHN3;SHN2 | Not available | Upstream | -286 |
Matrix_60 | AT1G01260;AT5G57150 | Not available | Upstream | -246 |
Matrix_65 | POC1;PIL1 | Not available | Upstream | -247 |
Matrix_7 | PIF4 | Not available | Upstream | -245 |
| | | Upstream | -246 |
| | | Upstream | -247 |
| | | Upstream | -248 |
Matrix_77 | PRR5 | Not available | Upstream | -244 |
Matrix_80 | BIM1 | Not available | Upstream | -246 |
| | | Upstream | -247 |
Matrix_91 | CRF3 | Not available | Upstream | -287 |
Motif_174 | SREATMSD | sugar-repressive element (SRE) found in 272 of the 1592 down-regulated genes after main stem decapitation in Arabidopsis | Upstream | -294 |
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 | -247 |
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 | -247 |
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 | -246 |
Motif_210 | REBETALGLHCB21 | REbeta found in Lemna gibba Lhcb21 gene promoter; Located at -114 to -109; A GATA sequence created at a position six nucleotides upstream could replace the function of REbeta; Required for phytochrome regulation | Upstream | -293 |
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 | -246 |
| | | Upstream | -247 |
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 | -231 |
| | | Upstream | -284 |
Motif_244 | ABRE-like binding site motif | Not available | Upstream | -245 |
| | | Upstream | -247 |
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 | -246 |
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 | -247 |
Motif_309 | GATA promoter motif | Arabidopsis thaliana GATA factors: organisation, expression and DNA-binding characteristics | Upstream | -227 |
Motif_339 | ABRE-like binding site motif | Molecular responses to dehydration and low temperature | Upstream | -247 |
Motif_448 | IRO2OS | OsIRO2-binding core sequence; G-box plus G; Transcription factor OsIRO2 is induced exclusively by Fe deficiency | Upstream | -247 |
Motif_459 | SORLIP1 | Identification of key promoter motifs involved in the network of light-regulated gene expression by combined analysis of genomic sequence and microarray data | Upstream | -280 |
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 | -301 |
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 | -245 |
Motif_558 | BOXIIPCCHS | Core of Box II/G box found in the parsley chs genes; Essential for light regulation | Upstream | -248 |
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 | -245 |
| | | Upstream | -248 |
Motif_638 | ABRE binding site motif | Not available | Upstream | -247 |
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 | -302 |
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 | -245 |
Motif_92 | ABREATRD22 | ABRE (ABA responsive element) in Arabidopsis dehydration-responsive gene rd22 | Upstream | -246 |