Matrix_32 | AHL25 | Not Available | | 87.17% |
Matrix_185 | AHL25 | Not Available | | 84.81% |
Matrix_54 | AHL20 | Not Available | | 83.98% |
Matrix_88 | AHL12 | Not Available | | 83.83% |
Matrix_125 | AHL12 | Not Available | | 83.40% |
Matrix_521 | AHL20 | Not Available | | 77.90% |
Matrix_212 | ATHB-12 | Not Available | | 76.99% |
Matrix_444 | AT1G19485; AT4G17950 | Not Available | | 75.79% |
Matrix_391 | AHL20 | Not Available | | 75.06% |
Matrix_131 | HDG12; EDT1; GL2; HDG8 | Not Available | | 71.92% |
Matrix_382 | AT3G04850 | Not Available | | 71.84% |
Matrix_284 | KAN2; KAN3; KAN; KAN4 | Not Available | | 71.22% |
Matrix_431 | ATHB21; HB-3 | Not Available | | 70.87% |
Matrix_341 | HMGA | Not Available | | 70.30% |
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) | | 68.82% |
Matrix_483 | ICU4 | Not Available | | 68.69% |
Matrix_114 | EPR1; AT3G10113 | Not Available | | 68.33% |
Matrix_354 | AHL12 | Not Available | | 68.25% |
Matrix_12 | EIN3; EIL2 | Not Available | | 68.07% |
Matrix_93 | YAB5 | Not Available | | 67.44% |
Matrix_17 | WRKY22 | Not Available | | 67.06% |
Matrix_308 | INO | Not Available | | 66.25% |
Matrix_434 | ARR11 | Not Available | | 65.59% |
Matrix_259 | AT1G50680; AT1G51120 | Not Available | | 65.51% |
Matrix_240 | AT4G29000 | Not Available | | 65.27% |
Matrix_286 | GATA7 | Not Available | | 65.18% |
Matrix_143 | GATA14; GATA6; GATA5 | Not Available | | 64.84% |
Matrix_351 | HAT9; ATHB-4; ATHB2; HAT22; HAT14 | Not Available | | 64.63% |
Matrix_75 | WRKY29 | Not Available | | 63.95% |
Matrix_70 | GATA26 | Not Available | | 63.80% |
Matrix_384 | ATWRKY17 | Not Available | | 63.38% |
Matrix_46 | AT4G21895 | Not Available | | 63.30% |
Matrix_495 | HD-GL2-1; ANL2 | Not Available | | 63.24% |
Matrix_268 | EMB2749; VND5; SMB; VND1; ANAC076; NAC101; ANAC105 | Not Available | | 63.17% |
Matrix_442 | AT5G62260 | Not Available | | 63.13% |
Matrix_99 | DOF4.7 | Not Available | | 63.11% |
Matrix_142 | ZFP8 | Not Available | | 62.85% |
Matrix_447 | RVE1 | Not Available | | 62.83% |
Matrix_231 | HDG2; HDG3; ATML1; HB-7 | Not Available | | 62.52% |
Matrix_313 | ATMYB65; MYB33 | Not Available | | 62.36% |
Matrix_333 | GATA3 | Not Available | | 62.03% |
Matrix_328 | AT1G76580 | Not Available | | 61.84% |
Matrix_370 | WRKY50; WRKY51 | Not Available | | 61.75% |
Matrix_249 | WRKY11 | Not Available | | 61.74% |
Matrix_181 | Dof5.7 | Not Available | | 61.73% |
Matrix_207 | WRKY10; WRKY57; AT2G44745; ATWRKY13; WRKY49 | Not Available | | 61.59% |
Matrix_380 | ATMYR1 | Not Available | | 61.51% |
Matrix_8 | KAN1 | Not Available | | 61.46% |
Matrix_81 | YAB1 | Not Available | | 61.34% |
Matrix_103 | ATHB1 | The Athb-1 and -2 HD-Zip domains homodimerize forming complexes of different DNA binding specificities | | 61.28% |
Matrix_227 | AT1G64620 | Not Available | | 61.22% |
Matrix_141 | AT3G25990 | Not Available | | 61.07% |
Matrix_435 | ATHB51 | Not Available | | 61.03% |
Matrix_263 | WRKY33; WRKY19; WRKY32 | Not Available | | 60.83% |
Matrix_500 | WRKY43 | Not Available | | 60.59% |
Matrix_441 | ATHB5 | Not Available | | 60.29% |
Matrix_416 | ASL5 | Not Available | | 60.18% |
Matrix_151 | ASIL1 | Not Available | | 60.09% |
Matrix_383 | CCA1 | Not Available | | 60.08% |
Matrix_206 | CUC1; ANAC100 | Not Available | | 59.98% |
Matrix_3 | WRKY48 | Not Available | | 59.95% |
Matrix_72 | CDF2 | Not Available | | 59.91% |
Matrix_160 | RVE1 | Not Available | | 59.67% |
Matrix_226 | GATA1 | Not Available | | 59.51% |
Matrix_453 | EIL3 | Not Available | | 59.51% |
Matrix_489 | RAV1 | Not Available | | 59.40% |
Matrix_157 | LHY; RVE2 | Not Available | | 59.39% |
Matrix_427 | ZAT14 | Not Available | | 59.31% |
Motif_615 | MARTBOX | T-Box; Motif found in SAR (scaffold attachment region; or matrix attachment region, MAR) | | 59.27% |
Motif_642 | SEF1MOTIF | SEF1 (soybean embryo factor 1) binding motif; sequence found in 5'-upstream region (-640; -765) of soybean beta-conglicinin (7S globulin) gene | | 59.03% |
Motif_277 | ATHB1 binding site motif | Recognition sequence of Arabidopsis Athb-1 protein; Athb-1 protein has a HD-Zip motif (homeodomain (HD) with a closely linked leucine zipper motif (Zip)); HD-Zip domain binds to DNA as a dimer; The Athb-1 and -2 HD-Zip domains homodimerize forming complexes of different DNA binding specificities | | 58.97% |
Matrix_4 | ARR14 | Not Available | | 58.87% |
Matrix_491 | AT1G68670; AT3G25790 | Not Available | | 58.86% |
Matrix_97 | APRR2 | Not Available | | 58.83% |
Matrix_276 | AT1G01520; AT3G09600; AT4G01280; LCL1; AT5G52660 | Not Available | | 58.61% |
Matrix_502 | AT3G13040 | Not Available | | 58.52% |
Matrix_102 | WRKY21 | Not Available | | 58.41% |
Matrix_461 | ATHB12 | Not Available | | 58.32% |
Motif_198 | CARGATCONSENSUS | CArG consensus sequence found in the promoter of Arabidopsis SOC1 which is the MADS-box flowering-time gene; FLC is a component of the vernalization (low-temperature) pathway binds directly to this site and blocks transcriptional activation of SOC1 by CONSTANS (CO) | | 58.26% |
Matrix_210 | ARR1 | Not Available | | 58.04% |
Matrix_100 | AT1G48610 | Not Available | | 57.94% |
Matrix_430 | TOE2 | Not Available | | 57.93% |
Matrix_423 | AT3G04030 | Not Available | | 57.91% |
Matrix_53 | MYC3 | Not Available | | 57.88% |
Matrix_56 | BZIP17; BZIP28; BZIP49 | Not Available | | 57.75% |
Matrix_112 | TBP2; TFIID-1 | Not Available | | 57.53% |
Matrix_37 | GATA27 | Not Available | | 57.49% |
Matrix_271 | AT3G16350 | Not Available | | 57.40% |
Matrix_418 | KNAT6; KNAT2 | Not Available | | 57.14% |
Matrix_62 | HAT5 | Not Available | | 57.02% |
Matrix_508 | APL; AT3G12730; AT3G24120; UNE16 | Not Available | | 57.02% |
Matrix_195 | GATA2; GATA4 | Not Available | | 56.86% |
Matrix_182 | ATHB6 | Not Available | | 56.84% |
Matrix_314 | WRKY65; WRKY14; WRKY35; WRKY69; WRKY16; ATWRKY52 | Not Available | | 56.80% |
Matrix_16 | AT3G04450; PHL1 | Not Available | | 56.78% |
Matrix_52 | ZAT18 | Not Available | | 56.74% |
Matrix_248 | ZFP5 | Not Available | | 56.73% |
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 | | 56.66% |
Matrix_204 | WOX13 | Not Available | | 56.64% |
Matrix_317 | AT1G06070; AT2G31370; AT2G40620 | Not Available | | 56.59% |
Motif_285 | HDZIP2ATATHB2 | Binding site of the Arabidopsis homeobox gene (ATHB-2) found in its own promoter; Located between -72 and -80; Similar to the HD-ZIP-2 binding consensus sequence; ATHB-2 is regulated by light signals which function as a negative autoregulator of its own gene | | 56.44% |
Matrix_59 | AT4G00238; AT4G00250 | Not Available | | 56.41% |
Matrix_162 | AtPHR1 | Not Available | | 56.35% |
Matrix_316 | WRKY15; WRKY39; WRKY7; WRKY74 | Not Available | | 56.35% |
Matrix_152 | EIL1; AT5G65100 | Not Available | | 56.07% |
Matrix_392 | ARR2 | Not Available | | 56.05% |
Matrix_318 | ATHB16 | Not Available | | 55.96% |
Matrix_175 | Dof5.7 | Not Available | | 55.83% |
Matrix_69 | AT2G03500 | Not Available | | 55.79% |
Matrix_71 | ATHB7 | Not Available | | 55.73% |
Matrix_408 | GATA12 | Not Available | | 55.58% |
Motif_352 | ATHB5 binding site motif | Consensus binding sequence for Arabidopsis class I HDzip (Homeodomein-leucine zipper) protein, ATHB5; ATHB5 protein forms dimers in solution; ATHB5 and ATHB6 exhibit identical DNA binding specificities; ATHB5 forms heterodimers with other class I HDzip proteins; DNA-binding and dimerization preferences of Arabidopsis homeodomain-leucine zipper transcription factors in vitro | | 55.56% |
Matrix_415 | WRKY27 | Not Available | | 55.50% |
Motif_83 | CIACADIANLELHC | Region necessary for circadian expression of tomato Lhc gene | | 55.42% |
Matrix_463 | HAT3.1 | Not Available | | 55.39% |
Matrix_241 | HB-1; AT5G44180 | Not Available | | 55.36% |
Matrix_311 | TGA1 | Not Available | | 55.36% |
Matrix_322 | NST3; ANAC015; BRN2 | Not Available | | 55.34% |
Matrix_280 | TCP24; TCP1; BRC2; ATTCP18 | Not Available | | 55.27% |
Matrix_410 | TOE2 | Not Available | | 55.23% |
Matrix_361 | AT1G25550 | Not Available | | 55.11% |
Matrix_177 | ADOF2 | Not Available | | 55.11% |
Matrix_324 | AT2G01060 | Not Available | | 55.09% |
Matrix_78 | AT3G45610 | Not Available | | 55.04% |
Matrix_230 | ARR11 | Not Available | | 54.88% |
Matrix_41 | anac058 | Not Available | | 54.56% |
Matrix_501 | DAG2 | Not Available | | 54.54% |
Matrix_302 | HAT1; HAT2 | Not Available | | 54.51% |
Matrix_256 | IXR11; KNAT5; KNAT4; KNAT3 | Not Available | | 54.46% |
Matrix_404 | OBP4 | Not Available | | 54.34% |
Matrix_220 | WRKY18 | Not Available | | 54.24% |
Matrix_366 | ARR14 | Not Available | | 54.10% |
Matrix_411 | DOF5.6 | Not Available | | 54.03% |
Matrix_327 | ARR11 | Not Available | | 54.00% |
Matrix_197 | NAP | Not Available | | 53.92% |
Matrix_402 | TOE1 | Not Available | | 53.88% |
Matrix_255 | cdf3 | Not Available | | 53.84% |
Matrix_265 | NGA3 | Not Available | | 53.81% |
Matrix_193 | RAV1 | Not Available | | 53.81% |
Matrix_38 | SPL14 | Not Available | | 53.78% |
Matrix_67 | GLK1 | Not Available | | 53.60% |
Matrix_397 | GT2L | Not Available | | 53.51% |
Matrix_202 | WRKY71; WRKY28; WRKY8 | Not Available | | 53.50% |
Matrix_452 | MYB46 | Not Available | | 53.45% |
Matrix_429 | KAN4 | Not Available | | 53.40% |
Matrix_101 | ERF5 | Not Available | | 53.19% |
Matrix_336 | AT5G08520 | Not Available | | 52.88% |
Matrix_26 | ATMYB3; MYB24 | Not Available | | 52.85% |
Matrix_171 | LBD3; LBD4 | Not Available | | 52.84% |
Matrix_84 | AtGRF6 | Not Available | | 52.63% |
Matrix_236 | CCA1 | Not Available | | 52.38% |
Matrix_166 | TGA4 | Not Available | | 52.24% |
Matrix_513 | SOL1; TSO1; TCX2 | Not Available | | 52.20% |
Matrix_519 | ATDOF2.4 | Not Available | | 52.18% |
Motif_169 | ATHB2 binding site motif | Recognition sequence of Arabidopsis Athb-2 protein; Athb-2 protein has a HD-Zip motif (homeodomain (HD) with a closely linked leucine zipper motif (Zip)); The Athb-1 and -2 HD-Zip domains homodimerize forming complexes of different DNA binding specificities | | 52.03% |
Matrix_350 | ARR14 | Not Available | | 52.03% |
Matrix_421 | GLK1 | Not Available | | 52.01% |
Matrix_128 | TGA2 | Not Available | | 51.92% |
Matrix_213 | ATHB22 | Not Available | | 51.90% |
Matrix_487 | AT1G29160 | Not Available | | 51.87% |
Matrix_329 | WRKY12 | Not Available | | 51.79% |
Matrix_357 | WRKY61; WRKY6; WRKY9; WRKY36; WRKY47; WRKY42; WRKY31; WRKY72 | Not Available | | 51.73% |
Matrix_87 | AT1G19000 | Not Available | | 51.69% |
Matrix_494 | OBP4 | Not Available | | 51.57% |
Matrix_293 | WRKY38 | Not Available | | 51.56% |
Matrix_106 | AT5G47390 | Not Available | | 51.40% |
Matrix_109 | GBF3 | Not Available | | 51.32% |
Matrix_254 | MYB52 | Not Available | | 51.25% |
Matrix_44 | CUC3; anac046; NAC3; ANAC087; ATNAC6; CUC2 | Not Available | | 51.21% |
Matrix_167 | ZAT6 | Not Available | | 51.15% |
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 | | 51.10% |
Matrix_471 | KAN4 | Not Available | | 51.04% |
Matrix_35 | YAB5; YAB3 | Not Available | | 51.01% |
Matrix_126 | RBE | Not Available | | 50.99% |
Matrix_274 | EDF3 | Not Available | | 50.97% |
Matrix_520 | ARR14 | Not Available | | 50.97% |
Matrix_479 | TOE1 | Not Available | | 50.90% |
Matrix_287 | ERF2 | Not Available | | 50.71% |
Matrix_505 | GATA8 | Not Available | | 50.70% |
Matrix_163 | AT2G20110 | Not Available | | 50.47% |
Matrix_198 | STZ; C2H2; AZF3 | Not Available | | 50.35% |
Matrix_9 | AT5G04760 | Not Available | | 50.34% |
Matrix_89 | SOC1 | Genome-wide identification of SOC1 and SVP targets during the floral transition in Arabidopsis | | 50.14% |
Motif_533 | Bellringer/replumless/pennywise BS3 IN AG | Repression of AGAMOUS by BELLRINGER in Floral and Inflorescence Meristems | | 50.10% |