Matrix_101 | ERF5 | Not available | Upstream | -1641 |
Matrix_120 | BEE2 | Not available | Upstream | -287 |
| | | Upstream | -288 |
Matrix_158 | AT1G03040;LRL1;UNE12;LRL2;LRL3 | Not available | Upstream | -287 |
| | | Upstream | -288 |
Matrix_186 | FHY3 | Not available | Upstream | -291 |
Matrix_196 | TCP20;AT5G41030 | Not available | Upstream | -377 |
| | | Upstream | -383 |
Matrix_224 | ERF1 | Not available | Upstream | -1640 |
Matrix_261 | ATERF-1 | Not available | Upstream | -1641 |
Matrix_277 | RAP2.6 | Not available | Upstream | -1640 |
Matrix_295 | ERF1 | Not available | Upstream | -1641 |
Matrix_323 | BIM3 | Not available | Upstream | -287 |
| | | Upstream | -288 |
Matrix_326 | AT5G07310;Rap2.6L;AT5G61890 | Not available | Upstream | -1640 |
Matrix_330 | MYC2;TT8 | Not available | Upstream | -287 |
| | | Upstream | -288 |
Matrix_333 | GATA3 | Not available | Upstream | -12 |
Matrix_334 | AT3G23230 | Not available | Upstream | -1642 |
Matrix_335 | HSFB2A | Not available | Upstream | -21 |
Matrix_339 | bHLH104 | Not available | Upstream | -287 |
| | | Upstream | -288 |
Matrix_343 | AT2G33710 | Not available | Upstream | -1641 |
Matrix_363 | RAP2.3 | Not available | Upstream | -1640 |
Matrix_369 | AT2G18300 | Not available | Upstream | -285 |
| | | Upstream | -286 |
| | | Upstream | -287 |
| | | Upstream | -288 |
Matrix_378 | ATERF1 | Not available | Upstream | -1641 |
Matrix_389 | ILR3 | Not available | Upstream | -287 |
| | | Upstream | -288 |
Matrix_426 | CRF1;CRF2 | Not available | Upstream | -1642 |
Matrix_449 | BIM2 | Not available | Upstream | -287 |
| | | Upstream | -288 |
Matrix_45 | DRN | Not available | Upstream | -1641 |
Matrix_465 | MYC4 | Not available | Upstream | -287 |
| | | Upstream | -288 |
Matrix_48 | PI | Not available | Upstream | -260 |
Matrix_484 | ATERF13 | Not available | Upstream | -1641 |
Matrix_488 | ABF1 | Not available | Upstream | -280 |
Matrix_506 | DRNL;ATERF-4 | Not available | Upstream | -1642 |
Matrix_90 | BEE1;BEE3;AT3G07340;AT5G48560;AT5G50915 | Not available | Upstream | -288 |
| | | Upstream | -289 |
Matrix_91 | CRF3 | Not available | Upstream | -1641 |
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 | -243 |
| | | Upstream | -288 |
Motif_256 | RHE_element | Functional Conservation of a Root Hair Cell-Specific cis-Element in Angiosperms with Different Root Hair Distribution Patterns | Upstream | -284 |
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 | -1641 |
Motif_339 | ABRE-like binding site motif | Molecular responses to dehydration and low temperature | Upstream | -242 |
| | | Upstream | -280 |
Motif_371 | DRE-like promoter motif | The Expression Profile Matrix of Arabidopsis Transcription Factor Genes Suggests Their Putative Functions in Response to Environmental Stresses | Upstream | -61 |
| | | Upstream | -148 |
Motif_48 | BES1 | A brassinosteroid transcriptional network revealed by genome-wide identification of BESI target genes in Arabidopsis thaliana | Upstream | -282 |
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 | -1103 |
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 | -195 |