Matrix_104 | PI | Not available | Upstream | -196 |
Matrix_108 | PIF4 | Interaction between BZR1 and PIF4 integrates brassinosteroid and environmental responses | Upstream | -196 |
Matrix_109 | GBF3 | Not available | Upstream | -196 |
| | | Upstream | -194 |
| | | Upstream | -128 |
Matrix_113 | ABI5 | Not available | Upstream | -196 |
| | | Upstream | -194 |
Matrix_118 | PIF3_2 | Direct targeting of light signals to a promoter element-bound transcription factor | Upstream | -198 |
| | | Upstream | -131 |
Matrix_120 | BEE2 | Not available | Upstream | -195 |
Matrix_122 | ABF1;AREB2 | Not available | Upstream | -196 |
| | | Upstream | -195 |
Matrix_129 | ABF1 | Not available | Upstream | -195 |
Matrix_134 | ABF1 | Not available | Upstream | -195 |
Matrix_14 | ZCW32;AT5G62610 | Not available | Upstream | -195 |
Matrix_145 | GBF4;AT5G44080 | Not available | Upstream | -194 |
Matrix_15 | PIF3_1 | Direct targeting of light signals to a promoter element-bound transcription factor | Upstream | -199 |
Matrix_156 | POC1 | Not available | Upstream | -196 |
| | | Upstream | -194 |
Matrix_158 | AT1G03040;LRL1;UNE12;LRL2;LRL3 | Not available | Upstream | -195 |
Matrix_169 | E2F1 | Not available | Upstream | -248 |
Matrix_192 | FHY3/FAR1 | Not available | Upstream | -198 |
Matrix_194 | HYH;HY5 | Not available | Upstream | -198 |
Matrix_200 | PIL5;AT4G28790;AT4G28800;AT4G28811;AT4G28815 | Not available | Upstream | -195 |
Matrix_206 | CUC1;ANAC100 | Not available | Upstream | -224 |
| | | Upstream | -199 |
Matrix_214 | AP1 | Not available | Upstream | -197 |
Matrix_217 | BES1 | A brassinosteroid transcriptional network revealed by genome-wide identification of BESI target genes in Arabidopsis thaliana | Upstream | -198 |
Matrix_23 | ANAC46 | Not available | Upstream | -200 |
Matrix_233 | MYC3 | Not available | Upstream | -194 |
Matrix_24 | POC1 | Not available | Upstream | -199 |
Matrix_247 | PIF3 | Not available | Upstream | -195 |
| | | Upstream | -127 |
Matrix_257 | NAC050;ANAC051;anac057;NAC2 | Not available | Upstream | -201 |
Matrix_259 | AT1G50680;AT1G51120 | Not available | Upstream | -195 |
| | | Upstream | -127 |
Matrix_264 | ATAREB1 | Not available | Upstream | -198 |
Matrix_296 | GBF2 | Not available | Upstream | -195 |
| | | Upstream | -194 |
| | | Upstream | -127 |
Matrix_300 | bZIP68;bZIP16 | Not available | Upstream | -195 |
| | | Upstream | -194 |
| | | Upstream | -127 |
Matrix_301 | PIL5 | Not available | Upstream | -200 |
Matrix_305 | PIF4 | Interaction between BZR1 and PIF4 integrates brassinosteroid and environmental responses | Upstream | -197 |
Matrix_308 | INO | Not available | Upstream | -228 |
Matrix_331 | GBF1 | Not available | Upstream | -196 |
| | | Upstream | -194 |
| | | Upstream | -128 |
Matrix_332 | SPT;ALC | Not available | Upstream | -195 |
| | | Upstream | -194 |
| | | Upstream | -127 |
Matrix_338 | AP2 | Not available | Upstream | -198 |
Matrix_345 | POC1 | Not available | Upstream | -198 |
| | | Upstream | -131 |
Matrix_356 | PRR5 | Not available | Upstream | -202 |
| | | Upstream | -198 |
Matrix_389 | ILR3 | Not available | Upstream | -195 |
Matrix_403 | BZR1 | Not available | Upstream | -197 |
Matrix_41 | anac058 | Not available | Upstream | -224 |
| | | Upstream | -199 |
Matrix_420 | ANAC58 | Not available | Upstream | -223 |
Matrix_44 | CUC3;anac046;NAC3;ANAC087;ATNAC6;CUC2 | Not available | Upstream | -199 |
Matrix_443 | AGL15 | Not available | Upstream | -197 |
Matrix_456 | bZIP60 | Not available | Upstream | -127 |
Matrix_475 | AT5G64220 | Not available | Upstream | -259 |
Matrix_480 | BES1 | Not available | Upstream | -196 |
Matrix_488 | ABF1 | Not available | Upstream | -263 |
Matrix_53 | MYC3 | Not available | Upstream | -257 |
| | | Upstream | -197 |
Matrix_55 | PIF3 | Not available | Upstream | -196 |
Matrix_56 | BZIP17;BZIP28;BZIP49 | Not available | Upstream | -196 |
| | | Upstream | -126 |
Matrix_60 | AT1G01260;AT5G57150 | Not available | Upstream | -194 |
Matrix_64 | PIF5 | Not available | Upstream | -194 |
Matrix_65 | POC1;PIL1 | Not available | Upstream | -194 |
| | | Upstream | -193 |
Matrix_7 | PIF4 | Not available | Upstream | -195 |
Matrix_77 | PRR5 | Not available | Upstream | -197 |
| | | Upstream | -196 |
Matrix_80 | BIM1 | Not available | Upstream | -256 |
| | | Upstream | -196 |
Motif_116 | INRNTPSADB | Inr (initiator) elements found in the tobacco psaDb gene promoter without TATA boxes; Light-responsive transcription of psaDb depends on Inr, but not TATA box | Upstream | -268 |
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 | -193 |
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 | -424 |
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 | -193 |
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 | -195 |
Motif_207 | MAMMALENHAN | Core sequence in enhancers from polyoma virus and from the IgM heavy chain gene | Upstream | -203 |
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 | -260 |
| | | Upstream | -253 |
| | | Upstream | -252 |
| | | Upstream | -194 |
| | | Upstream | -193 |
Motif_24 | CAMTA3 | Roles for Arabidopsis CAMTA transcription factors in cold-regulated gene expression and freezing tolerance | Upstream | -253 |
Motif_244 | ABRE-like binding site motif | Not available | Upstream | -195 |
| | | Upstream | -193 |
| | | Upstream | -182 |
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 | -195 |
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 | -259 |
| | | Upstream | -252 |
| | | Upstream | -244 |
Motif_336 | MYBMOUSE | Binding site for mouse c-myb protein | Upstream | -424 |
Motif_339 | ABRE-like binding site motif | Molecular responses to dehydration and low temperature | Upstream | -193 |
| | | Upstream | -180 |
| | | Upstream | -125 |
Motif_342 | POLASIG1 | PolyA signal; poly A signal found in legA gene of pea, rice alpha-amylase; -10 to -30 in the case of animal genes. Near upstream elements (NUE) in Arabidopsis | Upstream | -206 |
Motif_448 | IRO2OS | OsIRO2-binding core sequence; G-box plus G; Transcription factor OsIRO2 is induced exclusively by Fe deficiency | Upstream | -194 |
| | | Upstream | -193 |
Motif_473 | ABREOSRGA1 | ABRE (ABA responsive element) in rice RGA1 encoding a G protein alpha subunit;ABRE; ABA and water-stress responses; Found in maize rab28; maize rab28 is ABA-inducible in embryos and vegetative tissues; Found in the Arabidopsis (A.t.) alcohol dehydrogenase (Adh) gene promoter; ABRE2; Found in the maize (Z.m.) Cat1 gene promoter; Responsible for the induction by ABA; Binding site of CBF2; Arabidopsis CBF1 overexpression induces COR genes and enhances freezing tolerance; The CBF genes do not appear to be autoregulated through the CRT/DRE sequence;The cis-regulatory element CCACGTGG is involved in ABA and water-stress responses of the maize gene rab28. Characterization of a maize G-box binding factor that is induced by hypoxia | Upstream | -194 |
Motif_495 | TRANSINITMONOCOTS | Context sequence of translational initiation codon in monocots | Upstream | -226 |
Motif_502 | MYB98 | The MYB98 subcircuit of the synergid gene regulatory network includes genes directly and indirectly regulated by MYB98 | Upstream | -177 |
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 | -187 |
Motif_558 | BOXIIPCCHS | Core of Box II/G box found in the parsley chs genes; Essential for light regulation | Upstream | -195 |
Motif_570 | POLASIG2 | PolyA signal; poly A signal found in rice alpha-amylase; -10 to -30 in the case of animal genes | Downstream | 3418 |
Motif_599 | LREBOXIIPCCHS1;HY5 | BoxII; Light responsive element (LRE) found in the parsley CHS-1 (chalcone synthase-1) gene promoter; Required for light responsiveness; nuclear protein binding site; Highly conserved in various light inducible gene promoters; Arabidopsis bZIP protein HY5 directly interacts with light-responsive promoters in mediating light control of gene expression | Upstream | -195 |
Motif_618 | MYB1AT | MYB recognition site found in the promoters of the dehydration-responsive gene rd22 and many other genes in Arabidopsis | Upstream | -202 |
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 | -195 |
Motif_638 | ABRE binding site motif | Not available | Upstream | -195 |
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 | -188 |
| | | Upstream | -187 |
Motif_79 | UPRMOTIFIIAT | Motif II in the conserved UPR (unfolded protein response) cis-acting element in Arabidopsis genes coding for SAR1B, HSP-90, SBR-like, Ca-ATPase 4, CNX1, PDI, etc | Upstream | -208 |
Motif_88 | MYB2AT | Binding site for ATMYB2, an Arabidopsis MYB homolog; ATMYB2 binds oligonucleotides that contained a consensus MYB recognition sequence (TAACTG), such as is in the SV40 enhancer and the maize bronze-1 promoter; ATMYB2 is involved in regulation of genes that are responsive to water stress in Arabidopsis | Upstream | -424 |