Matrix_101 | ERF5 | Not available | Upstream | -125 |
| | | Upstream | -126 |
| | | Upstream | -299 |
Matrix_146 | ORA47 | Not available | Upstream | -125 |
| | | Upstream | -126 |
Matrix_147 | ERF3;AT1G80580 | Not available | Upstream | -125 |
| | | Upstream | -126 |
| | | Upstream | -299 |
Matrix_155 | RAP2.6;ERF110;ABR1 | Not available | Upstream | -300 |
Matrix_190 | ATERF1 | Not available | Upstream | -125 |
| | | Upstream | -126 |
Matrix_224 | ERF1 | Not available | Upstream | -125 |
Matrix_234 | RAP2.3 | Not available | Upstream | -125 |
| | | Upstream | -126 |
Matrix_261 | ATERF-1 | Not available | Upstream | -125 |
| | | Upstream | -126 |
Matrix_272 | DEAR4 | Not available | Upstream | -125 |
| | | Upstream | -126 |
Matrix_287 | ERF2 | Not available | Upstream | -125 |
| | | Upstream | -126 |
Matrix_288 | RAP2.3 | Not available | Upstream | -298 |
Matrix_326 | AT5G07310;Rap2.6L;AT5G61890 | Not available | Upstream | -125 |
Matrix_343 | AT2G33710 | Not available | Upstream | -125 |
| | | Upstream | -126 |
| | | Upstream | -299 |
Matrix_344 | ATERF15;AT4G18450 | Not available | Upstream | -125 |
| | | Upstream | -126 |
Matrix_355 | ERF10;ERF11 | Not available | Upstream | -125 |
| | | Upstream | -298 |
Matrix_360 | ORA59 | Not available | Upstream | -125 |
| | | Upstream | -126 |
Matrix_363 | RAP2.3 | Not available | Upstream | -298 |
Matrix_374 | AT5G07580;AT5G61590 | Not available | Upstream | -299 |
Matrix_406 | ATERF-7 | Not available | Upstream | -124 |
Matrix_409 | DEAR3 | Not available | Upstream | -125 |
Matrix_426 | CRF1;CRF2 | Not available | Upstream | -126 |
| | | Upstream | -127 |
Matrix_45 | DRN | Not available | Upstream | -125 |
| | | Upstream | -126 |
| | | Upstream | -299 |
Matrix_462 | ATERF-8 | Not available | Upstream | -124 |
Matrix_484 | ATERF13 | Not available | Upstream | -125 |
Matrix_493 | AT1G22985;AT1G71130 | Not available | Upstream | -125 |
| | | Upstream | -126 |
| | | Upstream | -299 |
Matrix_50 | ATERF14;AT5G43410 | Not available | Upstream | -125 |
Matrix_506 | DRNL;ATERF-4 | Not available | Upstream | -126 |
| | | Upstream | -127 |
Matrix_517 | ERF12 | Not available | Upstream | -125 |
| | | Upstream | -126 |
Matrix_86 | CRF5;CRF6;CRF4 | Not available | Upstream | -126 |
| | | Upstream | -127 |
Matrix_91 | CRF3 | Not available | Upstream | -125 |
| | | Upstream | -126 |
Motif_192 | BOXLCOREDCPAL | Consensus of the putative core sequences of box-L-like sequences in carrot; PAL1 promoter region; DCMYB1 bound to these sequences in vitro | Upstream | -157 |
Motif_193 | GLK1 | GLK transcription factors coordinate expression of the photosynthetic apparatus in Arabidopsis | Upstream | -153 |
Motif_254 | MYB46;MYB83 | MYB46 and MYB83 bind to the SMRE sites and directly activate a suite of transcription factors and secondary wall biosynthetic genes | Upstream | -157 |
Motif_292 | MYBPZM | Core of consensus maize P (myb homolog) binding site; 6 bp core; Maize P gene specifies red pigmentation of kernel pericarp, cob, and other floral organs; P binds to A1 gene, but not Bz1 gene; Maize C1 (myb homolog) activates both A1 and Bz1 genes | Upstream | -157 |
| | | Upstream | -829 |
Motif_305 | SP1SV40 | SP-1 binding site (GC box) in enhancer regions of SV40 and human metallothionein IIA (hMT IIA) | Upstream | -125 |
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 | -126 |
Motif_391 | REALPHALGLHCB21 | REalpha found in Lemna gibba Lhcb21 gene promoter; Located at -134 to -129; Binding site of proteins of whole-cell extracts; The DNA binding activity is high in etiolated plants but much lower in green plants; Required for phytochrome regulation | Upstream | -155 |
Motif_419 | MYB4 binding site motif | Not available | Upstream | -157 |
Motif_426 | MYB58;MYB63 | MYB58 and MYB63 are transcriptional activators of the lignin biosynthetic pathway during secondary cell wall formation in Arabidopsis | Upstream | -157 |
Motif_51 | MYB46 | Identification of a cis-acting regulatory motif recognized by MYB46, a master transcriptional regulator of secondary wall biosynthesis | Upstream | -157 |
Motif_531 | AP2SV40 | AP-2 binding site in enhancer regions of SV40 and human metallothionein IIA (hMT IIA) | Intron | 1849 |
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 | Intron | 1716 |
Motif_682 | GT1GMSCAM4 | GT-1 motif found in the promoter of soybean CaM isoform, SCaM-4; Plays a role in pathogen- and salt-induced SCaM-4 gene expression | Intron | 1716 |