Tag | Content |
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EnhancerAtlas ID | HS188-04535 |
Organism | Homo sapiens |
Tissue/cell | Th2 |
Coordinate | chr15:101873240-101875570 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Atoh1 | MA0461.2 | chr15:101875487-101875497 | AACATATGTT | + | 6.02 | Atoh1 | MA0461.2 | chr15:101875487-101875497 | AACATATGTT | - | 6.02 | ESR2 | MA0258.2 | chr15:101873442-101873457 | GGGCCAGTGTGACCT | - | 6.77 | Myod1 | MA0499.1 | chr15:101873461-101873474 | AAGGACAGCTGCT | - | 6.07 | SREBF1 | MA0595.1 | chr15:101873415-101873425 | ATCACCCCAC | + | 6.02 |
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| Number: 1 | ID | Chromosome | Start | End |
GH15I101333 | chr15 | 101873412 | 101875328 |
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Enhancer Sequence | AATATCATCG AAATAAGTCA ACTTGCAATT TGTAAGTCAA AGAGCATCTA TGCAATTAAT 60 TAACGCCTAT CTGCAGGCCG ACTCTGCTGC TGGCCACTGG TTTAAGCTTC TTCTTCTTCT 120 TTTTTTTAAC CACGGCATCC CCAGAATTCA GAGCAGGGTT ACTGTTTAGA AGGTCATCAC 180 CCCACATAGT TGAGGGGGCC AGGGGCCAGT GTGACCTGCC CAAGGACAGC TGCTCATGCT 240 GACGGGGCTC CCGGACGCCC CAGCCTTTCA ATGTTTGTTT CTAATTGGAT TGGCTCAATA 300 GGAAACACAT GCACACACAT GTTCAGCTGT GAACCCCCTC AGTGGGCCCT CATGACTGTC 360 TCCTGCGACC CAAGCTGGGG ACAGGGCCAT TGCTGGCTCA ATGTCTCTGT TGGCTGAAAA 420 ATCCCTGCTT CCTCTTCCTT TCCTGCCATG GGGTTTCTTG GCAATCAGAA TGGTTTCGGG 480 GAGGAAGAAT ACTGCTCTGA TTCTTTGCTG TTGACTGTGT TTTCTCAACA CTTACCTCTG 540 CCCATGCTCG CTACTCCACC CGCTGGCTCT AAATGGCAGC CTGTCTGTCT TTACATACCT 600 GCCTATGCAC TGTTTCTGCA ATGCAGGCCC CTCTGCCAGT ACAACTTTAC TTTTTGTTCC 660 AATTCTGGAA ATCTCTTAGC GTTTCTAAAT TCCAGAACAG GAGCTCCTGC TCATCCTCAT 720 ACCATAAGCC CATAGGCTGT AATCCACACC ATCCTGGGTG GGTGGGCGGG CAGGTGAAAG 780 ACAGGCGGGA CTGGCCCCAC TGGTGCGATT CGAAATGGCA TTCGACACTG ACCCATTTAC 840 ACAATGTGGC ATGTGGCAGC CCTGTTTCAT TTTAACCACA GCCTCAACTG GCTAAGTACT 900 AGGTTGCAAA AGGCTGGAGC CTGCACACTG TCCCAAGTCA GATTCTGTAC TGCCCAAGCC 960 TCCCTTAGCC TGGACAGGGC CGGAAGAGGT AAGCAAGGCC CTCCTACATG AAACAGCATC 1020 CCCAGCATAG CATTTCTAGC ACACGGTCTT CCACAGGGCT CGGTTCATTA AGCCCCACAG 1080 CAGCTCCCCC TCCCTGACAC AGTTCCTAAC CCAGCCTACG TGTGTGGTGA CAGCGACACA 1140 GGAAGTTGTT CTCACCGCTG CAGCAGTGAC ACAGGAAGTT GTTCTCACCG CTGCAGCAGT 1200 GACACAGGAA GTTGTTCTCA CCGCTGCAGC AGTGACACAG GAAGTTGTTC TCACCGCTGC 1260 AGCAGTGACA CAGGAAGTTG TTCTCACCGC TGCAGCAGTG ACACAGGAAG TTGTTCTCAC 1320 CGCTGCAGCA GTGACACAGG AAGTTGTTCT CACCGCTGCA GCAGTGACAC AGGAAGTTGT 1380 TCTCACCGCT GCAGCAGTGA CACAGGAAGT TGTTCTCACC GCTGCAGCAG TGACACAGGA 1440 AGTTGTTCTC ACCACTGCAG GTGCAGAAAA CAAGCCTGGT GAGGAACCTC TGACTCTCCT 1500 CAGCTCCTTA GGGTCCAGTT ACAGCCACAT TCCGACCACA AAGGAATCCG AGCACTTTAA 1560 CCACCAAGTG GTGCACTGAG ATTGGCTGGG GTTGTGATGA TGGTAGGACA GGGACCAAGG 1620 GCTCTAGAGG CTATCATTTG AGTTGAAGTT TATTTCAATT ATAGAGGATG TCTCCAAAAA 1680 CACCCACAAA AGGCCTGGTC ACCAAAACTG GATTTTTATT TTCAGATATA GTTTTGGTGG 1740 GACAAACAAG AGGGGCTGCT CCACACTCAG GGTCAGTGGT GTGCACTGTG TGGAAAAAGA 1800 GAGCAGGAAG AATTCCCAGG GACCCAGCAG ACAGGCAGCC TCATGGGAGG AGGCTGGACT 1860 GGAATGGAAG AGAGACTTCA TTATTATTAC ACTCTCTGTT TGACTTTATG TGTGTGTGTG 1920 TGTATGTGTG TATGTGTGTA TTTAGACAGG GTCTCACTCT GTTGCCTAGG CTGGAGTACA 1980 GTGGTACGAT CATGGCTCAC TGCAGCCCCA ACTTCCCAGG CTCAAGCCAT CCTCCCACCT 2040 CAGCATCCCA AGTGGCTAGG ACTACAGGTG TGCACCACCA CGCCCGGCTA CTTTTTGTAT 2100 TTTTGGTAGA GATAGAGTTT CACTATGTTT CTCAGGCTGG TCTCAAACTC CTGAGCTCAA 2160 GCGATCCTCC CACGTTGGCC TCCCAAAGTG TAGGATTTAC TGGTGTGAGC CACGCGCCCA 2220 GCCTGTTTGA CTTTTTGTTA AAACCACAAC ATATGTTACC TGTTCATATA TAAACATTAA 2280 AACTTTTTAA AAGTTTAATG TTTAAAATCT ATGAATAAAG TGGTTGTATG 2330
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