Matrix_101 | ERF5 | Not available | Upstream | -110 |
| | | Upstream | -73 |
Matrix_105 | SPL14 | Not available | Upstream | -84 |
| | | Upstream | -81 |
| | | Upstream | -80 |
Matrix_146 | ORA47 | Not available | Upstream | -110 |
Matrix_147 | ERF3;AT1G80580 | Not available | Upstream | -110 |
Matrix_154 | AT1G22190;AT1G36060;AT1G64380;RAP2.4;AT2G20880;AT2G22200;AT4G13620;AT4G28140;AT4G39780;AT5G65130 | Not available | Upstream | -75 |
Matrix_155 | RAP2.6;ERF110;ABR1 | Not available | Upstream | -72 |
Matrix_180 | SPL1 | Not available | Upstream | -76 |
Matrix_224 | ERF1 | Not available | Upstream | -111 |
Matrix_234 | RAP2.3 | Not available | Upstream | -110 |
Matrix_252 | RAP2.6 | Not available | Upstream | -110 |
Matrix_261 | ATERF-1 | Not available | Upstream | -110 |
| | | Upstream | -73 |
Matrix_287 | ERF2 | Not available | Upstream | -110 |
Matrix_295 | ERF1 | Not available | Upstream | -110 |
Matrix_326 | AT5G07310;Rap2.6L;AT5G61890 | Not available | Upstream | -111 |
| | | Upstream | -74 |
Matrix_334 | AT3G23230 | Not available | Upstream | -109 |
Matrix_342 | SPL14 | Identification of a Consensus DNA-Binding Site for the Arabidopsis thaliana SBP Domain Transcription Factor, AtSPL14, and Binding Kinetics by Surface Plasmon Resonance | Upstream | -81 |
Matrix_343 | AT2G33710 | Not available | Upstream | -110 |
Matrix_344 | ATERF15;AT4G18450 | Not available | Upstream | -110 |
Matrix_355 | ERF10;ERF11 | Not available | Upstream | -111 |
| | | Upstream | -74 |
Matrix_360 | ORA59 | Not available | Upstream | -110 |
Matrix_363 | RAP2.3 | Not available | Upstream | -111 |
Matrix_374 | AT5G07580;AT5G61590 | Not available | Upstream | -110 |
Matrix_377 | AT1G75490;DREB2C;AT2G40350;AT5G18450 | Not available | Upstream | -73 |
Matrix_378 | ATERF1 | Not available | Upstream | -110 |
Matrix_395 | AT1G19210;ORA47;AT4G31060;AT5G21960 | Not available | Upstream | -74 |
Matrix_406 | ATERF-7 | Not available | Upstream | -112 |
| | | Upstream | -75 |
Matrix_409 | DEAR3 | Not available | Upstream | -111 |
| | | Upstream | -74 |
Matrix_426 | CRF1;CRF2 | Not available | Upstream | -109 |
Matrix_45 | DRN | Not available | Upstream | -110 |
Matrix_450 | SPL7 | Not available | Upstream | -75 |
Matrix_462 | ATERF-8 | Not available | Upstream | -112 |
| | | Upstream | -75 |
Matrix_484 | ATERF13 | Not available | Upstream | -110 |
Matrix_493 | AT1G22985;AT1G71130 | Not available | Upstream | -110 |
| | | Upstream | -73 |
Matrix_50 | ATERF14;AT5G43410 | Not available | Upstream | -111 |
| | | Upstream | -74 |
Matrix_506 | DRNL;ATERF-4 | Not available | Upstream | -109 |
| | | Upstream | -72 |
Matrix_517 | ERF12 | Not available | Upstream | -110 |
Matrix_57 | WIN1;SHN3;SHN2 | Not available | Upstream | -111 |
Matrix_86 | CRF5;CRF6;CRF4 | Not available | Upstream | -109 |
Matrix_91 | CRF3 | Not available | Upstream | -110 |
| | | Upstream | -73 |
Motif_171 | TCP binding consensus | found enriched in peaks in chip-seq data for SEP3 | Upstream | -84 |
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 | -109 |
Motif_383 | UPRE-III(bZIP60) | The plant-specific transcription factor NAC103 is induced by bZIP60 through a new cis-regulatory element to modulate the unfolded protein response in Arabidopsis | Upstream | -114 |
Motif_392 | PALBOXAPC | Box A; Consensus; One of three putative cis-acting elements (boxes P, A, and L) of phenylalanine ammonia-lyase (PAL; EC 4.3.1.5) genes in parsley (P.c.); None of these elements (boxes P, A, and L) alone, or the promoter region containing all of them together, conferred elicitor or light responsiveness. These elements appear to be necessary but not sufficient for elicitor- or light-mediated PAL gene activation; See also Box P, Box L | Upstream | -73 |
Motif_437 | ANAERO2CONSENSUS | One of 16 motifs found in silico in promoters of 13 anaerobic genes involved in the fermentative pathway (anaerobic set 1) | Upstream | -163 |
Motif_454 | DRECRTCOREAT | Core motif of DRE/CRT (dehydration-responsive element/C-repeat) cis-acting element found in many genes in Arabidopsis and in rice; Os DREB1A bound to GCCGAC more preferentially than to ACCGAC whereas At DREB1A bound to both GCCGAC and ACCGAC efficiently; Maize ZmDREB1A bound to DRE; HaDREB2 in Helianthus annuus (sunflower) | Upstream | -127 |
Motif_525 | CRTDREHVCBF2 | Preferred sequence for AP2 transcriptional activator HvCBF2 of barley; Core CRT/DRE motif; HvCBF2 bound to a (G/a)(T/c)CGAC core motif; DNA binding is regulated by temperature | Upstream | -93 |
Motif_584 | UPRE-III(bZIP60) | The plant-specific transcription factor NAC103 is induced by bZIP60 through a new cis-regulatory element to modulate the unfolded protein response in Arabidopsis | Upstream | -114 |
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 | -127 |
| | | Upstream | -93 |