Tag | Content |
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EnhancerAtlas ID | HS087-01342 |
Organism | Homo sapiens |
Tissue/cell | HEK293T |
Coordinate | chr1:113044150-113046370 |
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 | GTATCAGCAT GGACTCATGG GTATTTAATT TTATGCTTTG GGTTACAATC GAAAACTGTT 60 TTGTTTTGTT GCCCAAATTG TCCAGCTTTG GCCACTGGGA ACTTTTCAGT TGGCTCCTGA 120 GTTTATGTTA ATTTTTAATA TGGATAGCTA TTACCCACAT AAACAAAAGC TCTTTGGGGT 180 CCTTGATAAT TTGTGAGTGT AAAGAGGTCC TGAGACCAAA ATGTTTGAGA ACCACCGCTC 240 TAGGGATCCT CTGGCTGACC CGAATCCCCG GTGTGTGTGC GCGCTTCGTC TGCAGGTAGG 300 AGTTGTGGTC TGGACAGAAG CAAAGTAGGC CACACTCGCC TGCCCTTGGG AACACCCACT 360 TCTCCGTGCC ACGCCCGCTC CTAAGGTTTT CTTCGGGCAG AAACGCGGGG ATCCCCAAGA 420 AGACGAAGCT CAGGCTGCCA TGCCTTTCCC GCGAACGCCA CGGCGCGGCG CCCGGTTCAC 480 AGGGCGAGTC GCCCACCCGC GAGTCGGAAA GCGCCCGGAA TCTTGGCTAA AGCTCAGCGT 540 TCTCCTCCGG GGCTGGGGCC CTGGCCAGGC CTGGCCTGAG CGGTCTCCCC TCACTCTGCG 600 GCTCGCTCTC CCGGGCTACT CCGGCGCGCA GGTGCTGCGC CCGCGGGAGA GAGCGATCCT 660 GCGGCCGTGG CGGACGCCGG GAGGAGCCAC CGGGCTCTCC TCTCAGGAGC GCGTCCCCGT 720 GCCCTCCAGC TGCCCGTCCC TGCTGAAAGC ATCCGGACAG CTCCCCGGGC CGCGGCCCTG 780 GGGCCCGCCA GAGCCCTGCC CTGCACCCCG CTCTCCCCTC TCTGGCCCGG AGGGCTGCGC 840 CGGGCAGATC CTTTCCTCTG CAAGACAGAG ACAAGCAGCG ATAAACAGCT AAAGCTGGAG 900 ACCCGGCTAA ATGATACAAT AAGTTCTCTA ATTGCCTCGA AAATAAGGTA ATGATTTGGC 960 AGAGGGAATG CTTTGATCTT ATCAGGCAAG AGAGACCTCT CCAAAGGAAA CCTCAGAGAA 1020 GGGCTGGAGG CCTCGGACTT GGGGGTGTGA AGCCCAAGGA CAGCCTGCTT TCCCCGCCCT 1080 CCCCCGACCC TGCGTGTCCA CGGTCCCCAG CCTCACCCTC CGGCTTTTCA TGGAAAGACC 1140 CTTCTCCTGT GATGACTGGA GGAGAGTACA CACACATAAC ACAGGGGTTA GGAGAGGAGG 1200 AGGGGGTGGG TTCTGGGTTT TTCAGGAACA GGAGGACGGC TGAAATGACT GGTGCAGTTT 1260 TAGAGAGGCT ATAGAGAAGG AAATTGGGGG AGAGGGGATT GCGGACAGGG ATTATGGAAA 1320 ACCTGACTTG GCTCAAGTCT GATGATGTTT CTTACACAGT GAGGGCTGCT GATTTGAGCT 1380 TTTCAGGCAG GAGGGAGTGA CAAAGGGAGG AGAACTTTGA GTGTCCTGCC TTCTCCAAGA 1440 ATCTGCACAC ACACTCACAC ACACACCATT GCTCTGCGCT GTGGGTGTCC CTGCCTGGCA 1500 GAGGCCCCAG CACAAAGAGG ATTAGAGAGA TGAGCTAATC TGGTTTGTAT CCCAGACATG 1560 GCCCCAGAAA GGGACCTTGT CCACCCTGAT ATGTAAGGAT GTGAAGGAGT GAGGAGTCTT 1620 TCTTTGGGGG CCTGCTGGCT AACAGTACCA GAGACCCCAC TCCACTGGAG TCCCTGGGAT 1680 ACTGCAGTCC TGACTTCAGG GTCAGATTTA GGAAGCAGAA AGACGGTCGG TCCCACAGAA 1740 GGAACTAGAT CTCTACCCTA CTTGTTTCAC CAGTGGGGAA ACTGAGGCCT GAAGTGGGAA 1800 AGTGATTTAC AGAGTCATGC CAATAGTGCA TGGCTGAGTT GGGGGAAAAA ACCCTCAGGT 1860 TTTCTGACTT TTTACTGGTC CAGTGCTCCC TGCACTGTGT TGCAGGAGCT GCAAGGGAGA 1920 GGTATGAGAC AGAGAGAGGG CAAGAGAAAG AGAGAGACGA AGACAGAAGC AAACATACAC 1980 ACCAAGGAAA ATAGAGGTGC GCACACACCC ACATGCACAG AGAGACGGAG AAAGCCACAG 2040 AGAGTCAGAA ACAACATGGA GAGACAGATG GAGAGAGTGA AGAAAGAGCA AGACAAACGG 2100 TCATACAGAT TCATACAGAG AGATACACAC GGAGAGACAG GGAGTGACAC AATCTGACAG 2160 GGAGACAGGC AAGAGACAGG GATTCAGAAA GAGAAGGACA GAGACATTCA GACAGGGAGG 2220
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