Tag | Content |
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EnhancerAtlas ID | HS139-02822 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr1:113044200-113046370 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Crx | MA0467.1 | chr1:113045664-113045675 | AAGAGGATTAG | + | 6.62 | HNF1A | MA0046.2 | chr1:113044275-113044290 | TGTTAATTTTTAATA | - | 6.03 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 2 | ID | Chromosome | Start | End |
GH01I112501 | chr1 | 113044223 | 113045387 | GH01I112503 | chr1 | 113046286 | 113049834 |
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Enhancer Sequence | GAAAACTGTT TTGTTTTGTT GCCCAAATTG TCCAGCTTTG GCCACTGGGA ACTTTTCAGT 60 TGGCTCCTGA GTTTATGTTA ATTTTTAATA TGGATAGCTA TTACCCACAT AAACAAAAGC 120 TCTTTGGGGT CCTTGATAAT TTGTGAGTGT AAAGAGGTCC TGAGACCAAA ATGTTTGAGA 180 ACCACCGCTC TAGGGATCCT CTGGCTGACC CGAATCCCCG GTGTGTGTGC GCGCTTCGTC 240 TGCAGGTAGG AGTTGTGGTC TGGACAGAAG CAAAGTAGGC CACACTCGCC TGCCCTTGGG 300 AACACCCACT TCTCCGTGCC ACGCCCGCTC CTAAGGTTTT CTTCGGGCAG AAACGCGGGG 360 ATCCCCAAGA AGACGAAGCT CAGGCTGCCA TGCCTTTCCC GCGAACGCCA CGGCGCGGCG 420 CCCGGTTCAC AGGGCGAGTC GCCCACCCGC GAGTCGGAAA GCGCCCGGAA TCTTGGCTAA 480 AGCTCAGCGT TCTCCTCCGG GGCTGGGGCC CTGGCCAGGC CTGGCCTGAG CGGTCTCCCC 540 TCACTCTGCG GCTCGCTCTC CCGGGCTACT CCGGCGCGCA GGTGCTGCGC CCGCGGGAGA 600 GAGCGATCCT GCGGCCGTGG CGGACGCCGG GAGGAGCCAC CGGGCTCTCC TCTCAGGAGC 660 GCGTCCCCGT GCCCTCCAGC TGCCCGTCCC TGCTGAAAGC ATCCGGACAG CTCCCCGGGC 720 CGCGGCCCTG GGGCCCGCCA GAGCCCTGCC CTGCACCCCG CTCTCCCCTC TCTGGCCCGG 780 AGGGCTGCGC CGGGCAGATC CTTTCCTCTG CAAGACAGAG ACAAGCAGCG ATAAACAGCT 840 AAAGCTGGAG ACCCGGCTAA ATGATACAAT AAGTTCTCTA ATTGCCTCGA AAATAAGGTA 900 ATGATTTGGC AGAGGGAATG CTTTGATCTT ATCAGGCAAG AGAGACCTCT CCAAAGGAAA 960 CCTCAGAGAA GGGCTGGAGG CCTCGGACTT GGGGGTGTGA AGCCCAAGGA CAGCCTGCTT 1020 TCCCCGCCCT CCCCCGACCC TGCGTGTCCA CGGTCCCCAG CCTCACCCTC CGGCTTTTCA 1080 TGGAAAGACC CTTCTCCTGT GATGACTGGA GGAGAGTACA CACACATAAC ACAGGGGTTA 1140 GGAGAGGAGG AGGGGGTGGG TTCTGGGTTT TTCAGGAACA GGAGGACGGC TGAAATGACT 1200 GGTGCAGTTT TAGAGAGGCT ATAGAGAAGG AAATTGGGGG AGAGGGGATT GCGGACAGGG 1260 ATTATGGAAA ACCTGACTTG GCTCAAGTCT GATGATGTTT CTTACACAGT GAGGGCTGCT 1320 GATTTGAGCT TTTCAGGCAG GAGGGAGTGA CAAAGGGAGG AGAACTTTGA GTGTCCTGCC 1380 TTCTCCAAGA ATCTGCACAC ACACTCACAC ACACACCATT GCTCTGCGCT GTGGGTGTCC 1440 CTGCCTGGCA GAGGCCCCAG CACAAAGAGG ATTAGAGAGA TGAGCTAATC TGGTTTGTAT 1500 CCCAGACATG GCCCCAGAAA GGGACCTTGT CCACCCTGAT ATGTAAGGAT GTGAAGGAGT 1560 GAGGAGTCTT TCTTTGGGGG CCTGCTGGCT AACAGTACCA GAGACCCCAC TCCACTGGAG 1620 TCCCTGGGAT ACTGCAGTCC TGACTTCAGG GTCAGATTTA GGAAGCAGAA AGACGGTCGG 1680 TCCCACAGAA GGAACTAGAT CTCTACCCTA CTTGTTTCAC CAGTGGGGAA ACTGAGGCCT 1740 GAAGTGGGAA AGTGATTTAC AGAGTCATGC CAATAGTGCA TGGCTGAGTT GGGGGAAAAA 1800 ACCCTCAGGT TTTCTGACTT TTTACTGGTC CAGTGCTCCC TGCACTGTGT TGCAGGAGCT 1860 GCAAGGGAGA GGTATGAGAC AGAGAGAGGG CAAGAGAAAG AGAGAGACGA AGACAGAAGC 1920 AAACATACAC ACCAAGGAAA ATAGAGGTGC GCACACACCC ACATGCACAG AGAGACGGAG 1980 AAAGCCACAG AGAGTCAGAA ACAACATGGA GAGACAGATG GAGAGAGTGA AGAAAGAGCA 2040 AGACAAACGG TCATACAGAT TCATACAGAG AGATACACAC GGAGAGACAG GGAGTGACAC 2100 AATCTGACAG GGAGACAGGC AAGAGACAGG GATTCAGAAA GAGAAGGACA GAGACATTCA 2160 GACAGGGAGG 2170
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