Matrix_119 | RRTF1 | Not available | Upstream | -60 |
Matrix_122 | ABF1;AREB2 | Not available | Upstream | -175 |
Matrix_126 | RBE | Not available | Upstream | -162 |
Matrix_129 | ABF1 | Not available | Upstream | -1769 |
Matrix_138 | RRTF1 | Not available | Upstream | -60 |
Matrix_14 | ZCW32;AT5G62610 | Not available | Upstream | -174 |
Matrix_186 | FHY3 | Not available | Upstream | -175 |
Matrix_217 | BES1 | A brassinosteroid transcriptional network revealed by genome-wide identification of BESI target genes in Arabidopsis thaliana | Upstream | -178 |
Matrix_252 | RAP2.6 | Not available | Upstream | -61 |
Matrix_264 | ATAREB1 | Not available | Upstream | -178 |
Matrix_285 | DDF1 | Not available | Upstream | -398 |
Matrix_288 | RAP2.3 | Not available | Upstream | -60 |
Matrix_295 | ERF1 | Not available | Upstream | -1050 |
Matrix_296 | GBF2 | Not available | Upstream | -175 |
Matrix_300 | bZIP68;bZIP16 | Not available | Upstream | -175 |
Matrix_301 | PIL5 | Not available | Upstream | -1055 |
Matrix_356 | PRR5 | Not available | Upstream | -182 |
Matrix_363 | RAP2.3 | Not available | Upstream | -60 |
Matrix_378 | ATERF1 | Not available | Upstream | -61 |
Matrix_403 | BZR1 | Not available | Upstream | -1058 |
Matrix_406 | ATERF-7 | Not available | Upstream | -1050 |
Matrix_416 | ASL5 | Not available | Upstream | -167 |
Matrix_426 | CRF1;CRF2 | Not available | Upstream | -8 |
Matrix_473 | RRTF1 | Not available | Upstream | -61 |
Matrix_484 | ATERF13 | Not available | Upstream | -1050 |
Matrix_53 | MYC3 | Not available | Upstream | -177 |
Matrix_77 | PRR5 | Not available | Upstream | -176 |
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 | -43 |
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 | -173 |
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 | -6 |
Motif_320 | AGCBOXNPGLB | AGC box repeated twice in a 61 bp enhancer element in tobacco class I beta-1,3-glucanase (GLB) gene;GCC-box; Binding sequence of Arabidopsis AtERFs; AtERF1,2 and 5 functioned as activators of GCC box-dependent transcription; AtERF3 and 4 acted as repressors; AtERF proteins are stress signal-response factors; EREBP2 binding site; Conserved in most PR-protein genes; Rice MAPK (BWMK1) phosphorylates OS EREBP1, which enhance DNA-binding activity of the factor to the GCC box | Upstream | -1050 |
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 | -46 |