Tag | Content |
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EnhancerAtlas ID | HS092-10656 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr11:120936760-120939060 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXA1 | MA0148.4 | chr11:120938236-120938252 | GTTTATTTACTTTGTG | - | 6.4 | MIXL1 | MA0662.1 | chr11:120937785-120937795 | TCTAATTAAC | + | 6.02 | Stat4 | MA0518.1 | chr11:120938503-120938517 | CTTCTAGGAAATAA | + | 6.11 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I121066 | chr11 | 120936729 | 120940535 |
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Enhancer Sequence | GAATACTGTG TGGCTTACAT AATAGAAAAG ATTAGAAAAT TAAGTTTGAG CAGGATTGAT 60 GGGAAGCAGG GTACAGCCAA GGTTTCTGTA TCTCGCTATA CAAACAATAT GCTTCTGACA 120 CTGGTCATTT TACAGTCATT AGTAAGTTGC TGGACTTCAT TGCCCTCAGA CACTTAAAGC 180 CGTGCTTTGA CTTCTTTGCT GTTCTGTATC TTGTGAATAA TCTCTGTTAG ACCTTGTGTC 240 CTTGCATTAC TCCTTAAGAG TTAAAATCCC AGTTATAGTT AGACAGGCTT ATATCAGCTT 300 CCCATGTTCT AGCTTCCAAG GAATGGAGAA AGAGAATATC TACTCCTCTT CAGTTTGTAT 360 AGTAGGAAGT GGTTCCTGCA TCTTACCTAT CTTTGGTTTT CTACCAATCA GAAGGGCATT 420 CAGATGCTGG ACAGCCAAAG TTGGCATATA TCTACTATAG TACCTGTTCC TTAGTAGTTG 480 TTGATACAAG TCCCCTGTGG AATTACCCAT TTACTCAGCA AATGTCTTTT GAGCCCTTGC 540 AGTATGCCAG GAACTGTTAG GCTTTTAAAA AGGAACTATA ATAGTATTCA TGCTGATGGC 600 CAGAGTGAGT GGCGAATAAC AACAGAGGAG TTGCATTAAA ATGTATTTGT TATGAAATAA 660 CGATATATAA ACAGAGTATT AGTATTATAC TTATCTCTTT CTCTTCCAAA TTATATCCAT 720 AATCTCTCCC TAAAATGTCA ATGAATAGCA CATAGTACTG TGTATAGTTA GTAAAAGGTG 780 GAATTTGACC CTCTACATCA TTCAGTGTCT CATATAAAAT TGAGCTTTAG TTTCCAGGTA 840 GGATGGAGGT ATCCATTTAT TTAAAGAAAA ACATTCTTTT TCATTTAATG AAATTTTTTT 900 AAAAATCAGT GTTCAGCTCA ATTTTCCTGT AAATTCTAAC TTCCACTACA GCCTTCCTAG 960 CTCGGTTCCC CGAGCTTTTC TTCCTCCTTT TATTTTCCTC TCGTGTCAGT TAAACATGAA 1020 ATAGCTCTAA TTAACTTTAA CATAAAGTAA GAAAAGTTAC CCAAAATGTC TTTGAGGTTA 1080 TGAATAAAGA GCCGACATGA TGAGCCGAAT GTCCTTTATG GTAGCAAAGT TATTTTGTGT 1140 GTCAGTTGGA TTATTTACAC ACATCTGTTT CTATGTGATT AGTCATTTTG GCAATAAAAG 1200 ACTTTAAAGA GGATCCAGAG ATTCACATAC CTGTTTTCCT ATCCCAGGAT GAAATGCAAA 1260 ATCTGAATCA TTTGAATTTT TATGATGAAA AGAGTAAAAT GTTTAGGAGA CTGAAGGGAG 1320 ACATACTTAT TAAGAGCTTT ATAATTTCTT ACAGGTGCTC AATTATCCTT TTTATTGCCT 1380 TCTGATAGGT AGAGCTGGAA GTTTAGCCTC TCTGCTCTAG CTGCTTATGG CAATAATGGA 1440 CTAACAAAAA ACTGAGCAAT CAGCCATATG TCTCATGTTT ATTTACTTTG TGAAACAAGA 1500 GAAGAGGAAA AATCTCTGTT TTCTGATTCT TGGCCTTTGA CCATCATACT GTTTGCTTTT 1560 CCAGTCAATG GACTCTTTTC TTTTAAAGCC GTCATCTGTG CCGTGTTTCT TAGTGGCTTA 1620 TATAGCAGTG GTGTGATATG CTGTTTCCAG ATAAGTTCAG TGTGTACTGC AGGTAGCTGG 1680 AAAGATGTCC TTACTGGGCT GGTCATATTT CAGTTATTAG ACTCTCAGGC CTTACCAGGA 1740 GAACTTCTAG GAAATAACTC TAGATTCTAG CTGGGTTTCA AAGGACAGTT TAATTTATTT 1800 ACTGAATACC TACTAAGGAC CAAGAGGCAC TGGGCTTCAA GCTAGAGATA AAGAGACAAA 1860 AACAGTAGTG TCTACTCTCA AGAAGCTAAG CTAGAGATAT ATTTCCTTTG CTGGGCCCTC 1920 TTCATGTTCC CAACCTCTAA AACTTGAGTT ACCCCAGGAC TTAGTCCTTG GACCTCTTCT 1980 CTTCTGTACT CATCCCCCAC ACACTTTTAG CCAGTCCCGA GGCTTTCAGT GCTTTCTGTA 2040 TTCTGATAAC TGCCAGATGT ATACATGCAG CTGTGATCTG CCTCTAAATT CCAGACGGCG 2100 CTTTCCAGCT GCCTGCTTGA TGCCTCTGCC TGGATGTTTA AACCTAGTGT GTCCAAAACT 2160 CAACTTTCGA TACCCTCCCT TTTCCCTTAC CCTGCCTCCC TCACCCCTAG CCCCCTGTGC 2220 CATAGCTACT GCTCTGCCAG TTTTTCTCCT TTTTTCAATT ATTCCAGTTG CTCAGGGAAA 2280 AAACACTGGA GTCATTCTTG 2300
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