Matrix_366 | ARR14 | Not Available | | 86.12% |
Matrix_408 | GATA12 | Not Available | | 80.77% |
Matrix_195 | GATA2; GATA4 | Not Available | | 80.06% |
Matrix_226 | GATA1 | Not Available | | 77.61% |
Matrix_447 | RVE1 | Not Available | | 76.07% |
Matrix_392 | ARR2 | Not Available | | 75.94% |
Matrix_157 | LHY; RVE2 | Not Available | | 75.68% |
Matrix_286 | GATA7 | Not Available | | 75.26% |
Matrix_391 | AHL20 | Not Available | | 75.23% |
Matrix_350 | ARR14 | Not Available | | 74.00% |
Matrix_502 | AT3G13040 | Not Available | | 73.47% |
Matrix_505 | GATA8 | Not Available | | 72.60% |
Matrix_203 | GATA9; GATA12 | Not Available | | 72.54% |
Matrix_283 | GATA15; GATA17; AT4G16141; GATA22; GATA23; GATA16; GNC | Not Available | | 71.26% |
Matrix_185 | AHL25 | Not Available | | 71.20% |
Matrix_67 | GLK1 | Not Available | | 70.61% |
Matrix_327 | ARR11 | Not Available | | 70.43% |
Matrix_271 | AT3G16350 | Not Available | | 70.29% |
Matrix_230 | ARR11 | Not Available | | 69.98% |
Matrix_37 | GATA27 | Not Available | | 69.71% |
Matrix_276 | AT1G01520; AT3G09600; AT4G01280; LCL1; AT5G52660 | Not Available | | 69.22% |
Matrix_88 | AHL12 | Not Available | | 69.09% |
Matrix_182 | ATHB6 | Not Available | | 68.50% |
Matrix_161 | MYBC1; AT3G10760; LUX; AT5G05090; AT5G59570 | Not Available | | 68.16% |
Matrix_361 | AT1G25550 | Not Available | | 66.62% |
Matrix_317 | AT1G06070; AT2G31370; AT2G40620 | Not Available | | 65.89% |
Matrix_491 | AT1G68670; AT3G25790 | Not Available | | 65.73% |
Matrix_324 | AT2G01060 | Not Available | | 65.65% |
Matrix_168 | AHL25 | Not Available | | 65.59% |
Matrix_336 | AT5G08520 | Not Available | | 65.42% |
Matrix_418 | KNAT6; KNAT2 | Not Available | | 65.39% |
Matrix_521 | AHL20 | Not Available | | 65.33% |
Matrix_16 | AT3G04450; PHL1 | Not Available | | 65.09% |
Matrix_106 | AT5G47390 | Not Available | | 64.47% |
Matrix_461 | ATHB12 | Not Available | | 64.46% |
Matrix_311 | TGA1 | Not Available | | 64.33% |
Matrix_114 | EPR1; AT3G10113 | Not Available | | 64.26% |
Matrix_522 | GATA11; GATA13 | Not Available | | 64.15% |
Matrix_302 | HAT1; HAT2 | Not Available | | 64.14% |
Matrix_256 | IXR11; KNAT5; KNAT4; KNAT3 | Not Available | | 64.05% |
Matrix_22 | BES1 | A brassinosteroid transcriptional network revealed by genome-wide identification of BESI target genes in Arabidopsis thaliana | | 63.91% |
Matrix_76 | GATA10 | Not Available | | 63.86% |
Matrix_69 | AT2G03500 | Not Available | | 63.85% |
Matrix_210 | ARR1 | Not Available | | 63.79% |
Matrix_4 | ARR14 | Not Available | | 63.55% |
Matrix_143 | GATA14; GATA6; GATA5 | Not Available | | 63.10% |
Matrix_512 | HAT3 | Not Available | | 63.04% |
Matrix_160 | RVE1 | Not Available | | 63.01% |
Matrix_308 | INO | Not Available | | 62.62% |
Matrix_162 | AtPHR1 | Not Available | | 62.56% |
Matrix_56 | BZIP17; BZIP28; BZIP49 | Not Available | | 62.51% |
Matrix_383 | CCA1 | Not Available | | 62.38% |
Matrix_351 | HAT9; ATHB-4; ATHB2; HAT22; HAT14 | Not Available | | 62.26% |
Matrix_463 | HAT3.1 | Not Available | | 62.18% |
Matrix_93 | YAB5 | Not Available | | 62.14% |
Matrix_71 | ATHB7 | Not Available | | 61.99% |
Matrix_508 | APL; AT3G12730; AT3G24120; UNE16 | Not Available | | 61.97% |
Motif_561 | GATA-2; GATA-4; GATA-3; GATA-1 | Arabidopsis thaliana GATA factors: organisation, expression and DNA-binding characteristics | | 61.92% |
Matrix_6 | AT1G70000 | Not Available | | 61.69% |
Matrix_333 | GATA3 | Not Available | | 61.52% |
Matrix_181 | Dof5.7 | Not Available | | 61.48% |
Matrix_63 | ARR10 | Not Available | | 61.36% |
Matrix_489 | RAV1 | Not Available | | 61.35% |
Matrix_72 | CDF2 | Not Available | | 61.34% |
Matrix_128 | TGA2 | Not Available | | 61.16% |
Matrix_354 | AHL12 | Not Available | | 61.09% |
Matrix_328 | AT1G76580 | Not Available | | 61.02% |
Matrix_212 | ATHB-12 | Not Available | | 60.71% |
Matrix_236 | CCA1 | Not Available | | 60.70% |
Matrix_32 | AHL25 | Not Available | | 60.51% |
Matrix_75 | WRKY29 | Not Available | | 60.46% |
Matrix_471 | KAN4 | Not Available | | 60.40% |
Matrix_125 | AHL12 | Not Available | | 60.30% |
Matrix_227 | AT1G64620 | Not Available | | 60.23% |
Matrix_518 | AT2G21230 | Not Available | | 60.23% |
Matrix_425 | TIFY2A | Not Available | | 60.19% |
Matrix_423 | AT3G04030 | Not Available | | 60.15% |
Matrix_17 | WRKY22 | Not Available | | 60.15% |
Matrix_404 | OBP4 | Not Available | | 60.11% |
Matrix_241 | HB-1; AT5G44180 | Not Available | | 60.03% |
Matrix_268 | EMB2749; VND5; SMB; VND1; ANAC076; NAC101; ANAC105 | Not Available | | 59.91% |
Matrix_109 | GBF3 | Not Available | | 59.89% |
Matrix_89 | SOC1 | Genome-wide identification of SOC1 and SVP targets during the floral transition in Arabidopsis | | 59.86% |
Matrix_231 | HDG2; HDG3; ATML1; HB-7 | Not Available | | 59.80% |
Matrix_504 | WRKY40 | Not Available | | 59.66% |
Matrix_432 | AT1G77920 | Not Available | | 59.34% |
Matrix_259 | AT1G50680; AT1G51120 | Not Available | | 59.33% |
Matrix_97 | APRR2 | Not Available | | 59.32% |
Matrix_70 | GATA26 | Not Available | | 59.29% |
Matrix_12 | EIN3; EIL2 | Not Available | | 59.24% |
Matrix_501 | DAG2 | Not Available | | 59.20% |
Matrix_255 | cdf3 | Not Available | | 59.02% |
Matrix_435 | ATHB51 | Not Available | | 58.99% |
Matrix_444 | AT1G19485; AT4G17950 | Not Available | | 58.98% |
Matrix_312 | ARF11; MP; ARF6; IAA21; ARF8; ARF4 | Not Available | | 58.91% |
Matrix_384 | ATWRKY17 | Not Available | | 58.89% |
Matrix_204 | WOX13 | Not Available | | 58.73% |
Matrix_218 | TIFY2B; TIFY1 | Not Available | | 58.63% |
Matrix_152 | EIL1; AT5G65100 | Not Available | | 58.60% |
Matrix_166 | TGA4 | Not Available | | 58.59% |
Matrix_263 | WRKY33; WRKY19; WRKY32 | Not Available | | 58.59% |
Matrix_206 | CUC1; ANAC100 | Not Available | | 58.54% |
Matrix_431 | ATHB21; HB-3 | Not Available | | 58.38% |
Matrix_313 | ATMYB65; MYB33 | Not Available | | 58.35% |
Matrix_103 | ATHB1 | The Athb-1 and -2 HD-Zip domains homodimerize forming complexes of different DNA binding specificities | | 58.09% |
Motif_464 | ARR1; ARR2 | Arabidopsis ARR1 and ARR2 response regulators operate as transcriptional activators | | 58.03% |
Matrix_207 | WRKY10; WRKY57; AT2G44745; ATWRKY13; WRKY49 | Not Available | | 57.70% |
Matrix_54 | AHL20 | Not Available | | 57.66% |
Matrix_53 | MYC3 | Not Available | | 57.63% |
Matrix_201 | AT1G74840 | Not Available | | 57.41% |
Motif_345 | GT-1 | Molecular dissection of GT-1 from Arabidopsis | | 57.40% |
Matrix_46 | AT4G21895 | Not Available | | 57.40% |
Matrix_3 | WRKY48 | Not Available | | 57.36% |
Matrix_483 | ICU4 | Not Available | | 57.25% |
Matrix_416 | ASL5 | Not Available | | 57.13% |
Matrix_167 | ZAT6 | Not Available | | 57.07% |
Matrix_347 | WOX14; WOX10 | Not Available | | 56.98% |
Matrix_370 | WRKY50; WRKY51 | Not Available | | 56.98% |
Matrix_331 | GBF1 | Not Available | | 56.98% |
Matrix_494 | OBP4 | Not Available | | 56.97% |
Matrix_141 | AT3G25990 | Not Available | | 56.92% |
Matrix_99 | DOF4.7 | Not Available | | 56.86% |
Matrix_284 | KAN2; KAN3; KAN; KAN4 | Not Available | | 56.82% |
Matrix_80 | BIM1 | Not Available | | 56.82% |
Motif_408 | EVENINGAT | Evening element found 46 times in the promoters of 31 cycling genes in Arabidopsis thaliana; Required for circadian control of gene expression; EE (evening element) motif; Also found in the promoter of the Solanum melongena gene encoding cysteine protease, and identified as cis-element for its circadian regulation;Orchestrated transcription of key pathways in Arabidopsis by the circadian clock | | 56.80% |
Matrix_87 | AT1G19000 | Not Available | | 56.51% |
Matrix_246 | ARR10 | Molecular structure of the GARP family of plant Myb-related DNA binding motifs of the Arabidopsis response regulators | | 56.35% |
Matrix_101 | ERF5 | Not Available | | 56.33% |
Matrix_8 | KAN1 | Not Available | | 56.25% |
Matrix_419 | TGA9; PAN; TGA6; bZIP65 | Not Available | | 56.20% |
Matrix_453 | EIL3 | Not Available | | 55.86% |
Matrix_429 | KAN4 | Not Available | | 55.84% |
Matrix_265 | NGA3 | Not Available | | 55.84% |
Matrix_193 | RAV1 | Not Available | | 55.84% |
Matrix_441 | ATHB5 | Not Available | | 55.83% |
Matrix_254 | MYB52 | Not Available | | 55.66% |
Matrix_279 | HRS1 | Not Available | | 55.64% |
Matrix_430 | TOE2 | Not Available | | 55.63% |
Matrix_274 | EDF3 | Not Available | | 55.52% |
Matrix_38 | SPL14 | Not Available | | 55.35% |
Matrix_62 | HAT5 | Not Available | | 55.28% |
Matrix_520 | ARR14 | Not Available | | 55.26% |
Matrix_410 | TOE2 | Not Available | | 55.15% |
Matrix_380 | ATMYR1 | Not Available | | 55.14% |
Matrix_296 | GBF2 | Not Available | | 55.03% |
Matrix_126 | RBE | Not Available | | 54.98% |
Matrix_51 | LFY | Not Available | | 54.96% |
Matrix_322 | NST3; ANAC015; BRN2 | Not Available | | 54.92% |
Matrix_59 | AT4G00238; AT4G00250 | Not Available | | 54.92% |
Matrix_81 | YAB1 | Not Available | | 54.86% |
Matrix_151 | ASIL1 | Not Available | | 54.82% |
Matrix_507 | TCP3 | Not Available | | 54.79% |
Motif_637 | SARD1; CBP60g | Control of salicylic acid synthesis and systemic acquired resistance by two members of a plant-specific family of transcription factors | | 54.77% |
Matrix_442 | AT5G62260 | Not Available | | 54.75% |
Matrix_421 | GLK1 | Not Available | | 54.67% |
Motif_43 | CCA1 binding site motif | CCA1 binding site; CCA1 protein (myb-related transcription factor) interact with two imperfect repeats of AAMAATCT in Lhcb1*3 gene of Arabidopsis thaliana; Related to regulation by phytochrome;A myb-related transcription factor is involved in the phytochrome regulation of an Arabidopsis Lhcb gene | | 54.56% |
Matrix_171 | LBD3; LBD4 | Not Available | | 54.51% |
Matrix_303 | ATWOX13 | Not Available | | 54.41% |
Matrix_85 | SPL5 | Not Available | | 54.35% |
Matrix_21 | HSFC1 | Not Available | | 54.30% |
Matrix_402 | TOE1 | Not Available | | 54.28% |
Matrix_113 | ABI5 | Not Available | | 54.24% |
Matrix_523 | FUSCA3 | Not Available | | 54.24% |
Matrix_300 | bZIP68; bZIP16 | Not Available | | 54.23% |
Matrix_205 | AGL15 | Not Available | | 54.19% |
Matrix_287 | ERF2 | Not Available | | 54.15% |
Matrix_318 | ATHB16 | Not Available | | 54.08% |
Matrix_131 | HDG12; EDT1; GL2; HDG8 | Not Available | | 54.03% |
Matrix_78 | AT3G45610 | Not Available | | 53.97% |
Matrix_479 | TOE1 | Not Available | | 53.95% |
Motif_582 | ARR1; ARR2 | Arabidopsis ARR1 and ARR2 response regulators operate as transcriptional activators | | 53.88% |
Matrix_280 | TCP24; TCP1; BRC2; ATTCP18 | Not Available | | 53.86% |
Matrix_198 | STZ; C2H2; AZF3 | Not Available | | 53.85% |
Matrix_248 | ZFP5 | Not Available | | 53.82% |
Matrix_379 | RHL41 | Not Available | | 53.81% |
Matrix_515 | ddf2; ATCBF3; CBF1; CBF4 | Not Available | | 53.68% |
Matrix_84 | AtGRF6 | Not Available | | 53.68% |
Matrix_102 | WRKY21 | Not Available | | 53.65% |
Motif_424 | GATA-1 | Arabidopsis thaliana GATA factors: organisation, expression and DNA-binding characteristics | | 53.56% |
Matrix_164 | AT1G02030; AT2G45120; AZF2; AT3G60580 | Not Available | | 53.55% |
Matrix_175 | Dof5.7 | Not Available | | 53.52% |
Matrix_139 | OBF5 | Not Available | | 53.50% |
Matrix_415 | WRKY27 | Not Available | | 53.31% |
Matrix_503 | AT2G37430; AT3G53600 | Not Available | | 53.25% |
Matrix_481 | BES1 | A brassinosteroid transcriptional network revealed by genome-wide identification of BESI target genes in Arabidopsis thaliana | | 53.22% |
Matrix_424 | MYB59 | Not Available | | 53.20% |
Matrix_239 | AT5G04390 | Not Available | | 53.13% |
Matrix_397 | GT2L | Not Available | | 53.01% |
Matrix_178 | HSFB2A | Not Available | | 53.00% |
Matrix_341 | HMGA | Not Available | | 52.88% |
Matrix_26 | ATMYB3; MYB24 | Not Available | | 52.87% |
Matrix_519 | ATDOF2.4 | Not Available | | 52.80% |
Motif_347 | OPAQUE2ZMB32 | opaque-2 binding site of maize b-32 (type I ribosome-inactivating protein gene); O2; O2S; O2S and GARE form a gibberellin response complex (GARC) | | 52.73% |
Matrix_44 | CUC3; anac046; NAC3; ANAC087; ATNAC6; CUC2 | Not Available | | 52.69% |
Motif_624 | ATHB6 binding site motif | Consensus binding sequence for Arabidopsis homeodomain-leucine zipper protein, ATHB6; ATHB6 is a target of the protein phosphatase ABI1 and regulates hormone responses; Homeodomain protein ATHB6 is a target of the protein phosphatase ABI1 and regulates hormone responses in Arabidopsis | | 52.68% |
Matrix_436 | AT3G49930; AZF1 | Not Available | | 52.54% |
Matrix_41 | anac058 | Not Available | | 52.47% |
Matrix_122 | ABF1; AREB2 | Not Available | | 52.28% |
Matrix_199 | AT1G69170; SPL9; SPL15; SPL13A; SPL13B | Not Available | | 52.27% |
Matrix_165 | KNAT1 | Not Available | | 52.25% |
Matrix_177 | ADOF2 | Not Available | | 52.20% |
Matrix_188 | SPL4 | Not Available | | 51.99% |
Matrix_142 | ZFP8 | Not Available | | 51.89% |
Motif_34 | LECPLEACS2 | Core element in LeCp (tomato Cys protease) binding cis-element (from -715 to -675) in LeAcs2 gene | | 51.72% |
Matrix_14 | ZCW32; AT5G62610 | Not Available | | 51.68% |
Matrix_9 | AT5G04760 | Not Available | | 51.67% |
Matrix_258 | WOX13 | Not Available | | 51.48% |
Matrix_58 | WRKY55; ATWRKY54; WRKY46; WRKY70; AtWRKY41; WRKY53; WRKY30 | Not Available | | 51.44% |
Matrix_427 | ZAT14 | Not Available | | 51.34% |
Matrix_399 | TGA1 | Not Available | | 51.32% |
Matrix_243 | RAP2.12; RAP2.2 | Not Available | | 51.31% |
Matrix_315 | MYB111 | Not Available | | 51.30% |
Motif_235 | C8GCARGAT | Binding site of plant MADS-domain protein AGL15; CArG motif with a longer A/T-rich core;A variant of CArG motif, with a longer A/T-rich core; Binding site for AGL15 (AGAMOUS-like 15) | | 51.30% |
Motif_677 | AGL22; AGL20; AGL24 | Regulation of floral patterning by flowering time genes | | 51.28% |
Matrix_220 | WRKY18 | Not Available | | 51.28% |
Motif_83 | CIACADIANLELHC | Region necessary for circadian expression of tomato Lhc gene | | 51.24% |
Matrix_412 | GL1 | Not Available | | 51.23% |
Matrix_197 | NAP | Not Available | | 51.16% |
Matrix_411 | DOF5.6 | Not Available | | 51.11% |
Motif_580 | L1BOXATPDF1 | L1 box found in promoter of Arabidopsis thaliana PROTODERMAL FACTOR1 (PDF1) gene; Located between -134 and -127; Involved in L1 layer-specific expression; L1-specific homeodomain protein ATML can bind to the L1 box; Y=C/T; A cotton fiber gene, RD22-like 1 (RDL1), contains a homeodomain binding L1 box and a MYB binding motif ; HDZip IV; Identification of a cis-regulatory element for L1 layer-specific gene expression, which is targeted by an L1-specific homeodomain protein | | 51.03% |
Motif_540 | CCA1 motif1 BS in CAB1 | A myb-related transcription factor is involved in the phytochrome regulation of an Arabidopsis Lhcb gene | | 51.00% |
Matrix_319 | TEM1 | Not Available | | 50.95% |
Matrix_52 | ZAT18 | Not Available | | 50.57% |
Matrix_202 | WRKY71; WRKY28; WRKY8 | Not Available | | 50.52% |
Matrix_40 | TCP2 | Not Available | | 50.37% |
Motif_475 | GATA-1 | Arabidopsis thaliana GATA factors: organisation, expression and DNA-binding characteristics | | 50.31% |
Matrix_420 | ANAC58 | Not Available | | 50.29% |
Matrix_25 | AP3 | Not Available | | 50.20% |
Matrix_406 | ATERF-7 | Not Available | | 50.14% |
Matrix_368 | ATWRKY56; WRKY45; WRKY75; WRKY24 | Not Available | | 50.10% |
Motif_131 | P1BS | PHR1-binding sequence found in the upstream regions of phosphate starvation responsive genes from several plant species; phr1 (phosphate starvation response 1) gene codes for PHR1 protein related to PSR1 gene in C. reinhardtii | | 50.04% |