Matrix_108 | PIF4 | Interaction between BZR1 and PIF4 integrates brassinosteroid and environmental responses | Upstream | -191 |
| | | Upstream | -755 |
Matrix_109 | GBF3 | Not available | Upstream | -193 |
Matrix_113 | ABI5 | Not available | Upstream | -191 |
| | | Upstream | -757 |
Matrix_122 | ABF1;AREB2 | Not available | Upstream | -756 |
Matrix_129 | ABF1 | Not available | Upstream | -192 |
| | | Upstream | -756 |
Matrix_133 | DYT1 | Not available | Upstream | -187 |
Matrix_15 | PIF3_1 | Direct targeting of light signals to a promoter element-bound transcription factor | Upstream | -188 |
Matrix_153 | AP2 | Not available | Upstream | -191 |
Matrix_156 | POC1 | Not available | Upstream | -193 |
| | | Upstream | -755 |
| | | Upstream | -757 |
Matrix_200 | PIL5;AT4G28790;AT4G28800;AT4G28811;AT4G28815 | Not available | Upstream | -756 |
Matrix_216 | TCP16 | Not available | Upstream | -1057 |
Matrix_217 | BES1 | A brassinosteroid transcriptional network revealed by genome-wide identification of BESI target genes in Arabidopsis thaliana | Upstream | -149 |
| | | Upstream | -150 |
Matrix_24 | POC1 | Not available | Upstream | -188 |
Matrix_266 | TCP16 | Determinants of the DNA binding specificity of class I and class II TCP transcription factors | Upstream | -1057 |
Matrix_301 | PIL5 | Not available | Upstream | -187 |
| | | Upstream | -757 |
Matrix_331 | GBF1 | Not available | Upstream | -193 |
Matrix_359 | FLC | Not available | Upstream | -754 |
Matrix_403 | BZR1 | Not available | Upstream | -190 |
| | | Upstream | -754 |
Matrix_438 | AtbZIP63 | Not available | Upstream | -756 |
Matrix_488 | ABF1 | Not available | Upstream | -748 |
Matrix_55 | PIF3 | Not available | Upstream | -191 |
| | | Upstream | -755 |
Matrix_56 | BZIP17;BZIP28;BZIP49 | Not available | Upstream | -757 |
Matrix_64 | PIF5 | Not available | Upstream | -193 |
| | | Upstream | -757 |
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 |
| | | Upstream | -757 |
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 | -193 |
| | | Upstream | -756 |
| | | Upstream | -1045 |
Motif_244 | ABRE-like binding site motif | Not available | Upstream | -152 |
| | | Upstream | -193 |
Motif_307 | TATCCAYMOTIFOSRAMY3D | TATCCAY motif found in rice RAmy3D alpha-amylase gene promoter; a GATA motif as its antisense sequence; TATCCAY motif and G motif are responsible for sugar repression | Upstream | -137 |
Motif_339 | ABRE-like binding site motif | Molecular responses to dehydration and low temperature | Upstream | -154 |
| | | Upstream | -193 |
| | | Upstream | -757 |
Motif_34 | LECPLEACS2 | Core element in LeCp (tomato Cys protease) binding cis-element (from -715 to -675) in LeAcs2 gene | Upstream | -141 |
Motif_346 | SND1;VND6;VND7;NST1;NST2 | Global analysis of direct targets of secondary wall NAC master switches in Arabidopsis | Upstream | -142 |
Motif_448 | IRO2OS | OsIRO2-binding core sequence; G-box plus G; Transcription factor OsIRO2 is induced exclusively by Fe deficiency | Upstream | -193 |
| | | Upstream | -756 |
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 | -151 |
| | | Upstream | -534 |
| | | Upstream | -786 |
Motif_543 | TATCCACHVAL21 | TATCCAC box is a part of the conserved cis-acting response complex (GARC) that most often contain three sequence motifs, the TAACAAA box, or GA-responsive element (GARE); the pyrimidine box, CCTTTT (see S000259); and the TATCCAC box, which are necessary for a full GA response | Upstream | -137 |
Motif_558 | BOXIIPCCHS | Core of Box II/G box found in the parsley chs genes; Essential for light regulation | Upstream | -152 |
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 | -169 |
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 | -152 |
Motif_628 | TATCCAOSAMY | TATCCA element found in alpha-amylase promoters of rice at positions ca.90 to 150bp upstream of the transcription start sites; Binding sites of OsMYBS1, OsMYBS2 and OsMYBS3 which mediate sugar and hormone regulation of alpha-amylase gene expression; See also AMYBOX2 | Upstream | -138 |
Motif_638 | ABRE binding site motif | Not available | Upstream | -152 |