Tag | Content |
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EnhancerAtlas ID | HS118-18537 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr8:97304510-97305930 |
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) |
HLTF | MA0109.1 | chr8:97304545-97304555 | AACCTTATAT | + | 6.02 | TFAP2A | MA0003.3 | chr8:97304749-97304760 | TGCCTGAGGCT | - | 6.32 |
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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: 1 | ID | Chromosome | Start | End |
GH08I096293 | chr8 | 97305500 | 97306614 |
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Enhancer Sequence | CTGTCTCAAA AAAAAAAAAA AAAAAAAAGA AAAGAAACCT TATATTTAAA GTGCTATACA 60 TTGTAATATA TTGAAATAGT CACCCTAATT CTCAAAACAA TACAGTGTGA AAAAGACGTG 120 TCATAGATTC AAGGAAGCAC GATAGTTAAA AATGGTACAG TCTGTGTAGA GGTCCTGATT 180 GGGGGTGTGG GGAGCTGGGA CCAGTCTGAG CTGGGACCAG ATCATGAGGC AGAGGGCCCT 240 GCCTGAGGCT AGGAGGCTGC CAGGGCTGAG CCAGCTGGGA TGAGGAGTTT AGGTGTTATT 300 CTAAGTGTAT GAAAAGGCCA TGGAAGGTTT ATAAGCAGAG GAGCTACATG ACCTGTGTTG 360 ATGTTTTAGG AGGTCAATCA ATAAATACCT CCATTTCTAG TTGAGTTTGG AAACAGAAAC 420 AAGAGTTCAA AATCTCAGCT GATTTCTTCC TGTGAAAGCT CAGTGGAGCA GATTGCTTTA 480 GACCTGGGCT GAATTAAGCA AGCCTGTCTT CCCCTAGCCC ATTAGACAAC CACAAGCTGC 540 TTCTGCAAAG CAGGGCCTGA CCCACAAAAA TTGCTGCATG GCTGGGGGAG CTGATGAGAA 600 CCTGTGCTGT CTGTAAGCAA ATAATTTCCA AAGAGGACCC AAAAGAGGTT GGATCTCTTT 660 CTTCTTCCAA AGTCAGCAAC TGCCCCAGAG AGGAGTGAAG AGATAGTTGG GCTGGAGACC 720 TGGCGTGTGT AGTAGTGGAG ATCCTTCTAC ATTGGGACGG GCATGCTACC CAACCCCTTT 780 CTTCCCACCT CCTGCCCCAG ACACCCTTAC ACACATGCAT GCACGTTCCG TGATCTGATT 840 ATGATTTTCA AGATCTCTCT GTAGTCGTAA GCTAGATGTG AATACCTAGG TGCTTATTAT 900 AGCATCATCT ATACTTTGTT ATATGCCTGA CACATTCCAC AGTTTTCAAA AGCTATTATT 960 ATGGAAGTCT AAGCAAGAAA TAATAGTGGC AGCGAGATGC ATAAAAGAAC AACCTGGGGA 1020 GGTAAAGTGA ATAGGACTTG GTATTTGGTT AGGTGTCCAG CAAGCAAGGC AGAGGGTAAG 1080 GCCGCCAAGA TCAGCCTAGG ACCAGTTGGG AAGTCAGCAG AATCTGTCTT TACCCATCTT 1140 TTGCTCACAG GCATGCACCT GTCCACTTGA CCCCCTTTCC AGGCTTCAGC TCTACACTGT 1200 CTTCAGTTAA AGCCTGTTCC TCCTGGTTCC CAGGGTTCTG CCTGCATGCA GCTCTCTGGC 1260 TGCTTTAAAC TGCAATGCCC TGTGGCCCTT CCAGGACAAG GACCTCAGGT CTTATGAGGG 1320 GATAATTGGC AAATCTGTTC ATTACTAACT ATACTGCAAA TAGACGGATT GGTCTTTATG 1380 ATTTTTAAAA TGCCTTTCCG CATGTCAAAG CATAGAGCTA 1420
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