Tag | Content |
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EnhancerAtlas ID | HS118-18051 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr8:17204710-17206460 |
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) |
HSF1 | MA0486.2 | chr8:17204968-17204981 | GAAGCTTCTAGAA | - | 6.28 |
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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 |
GH08I017347 | chr8 | 17204976 | 17209403 |
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Enhancer Sequence | AAAAAAAAAA ATCACATCTT CCTTTGCCTC TAACCAGTGC TCCAGCTCTG TGCAAGCTGA 60 AATACATTCA GAGTTAATAA AATACTTTAG ACCCTAATTC AAGGCTAGGA AAAGAAGAAG 120 AGCAATGAGT ATAACTAAAA ATAATTTTTA TCCAATTCAC AGAACTTTCA CCACCAAATT 180 AATATTTTCC TTCAAAGTAG CAACAGAGAG GGCTATGTGC TCACTCTGAT GAAGCTGGCA 240 TTGCTCCAGA TATTTTTGGA AGCTTCTAGA ATCTGACTGA GACCCTGCTC TACCCCCCGG 300 CTGTAGGTGC AGGCATGTGG ATACACACTC ACACAATCTC CTGTGTTTAT AGCCTCACTC 360 GGCTTTGAAT CCAGAAGTAT ATTATCTAGC TTAAAAACTA AAGTTTCTCT CTCACCTTGC 420 TAGAACCAAA GAACATTTTG TTTTTTTAAA CCACCTTTTT TAAAGGTGGT TTTTTGCTAC 480 CTTTTAAAAG TGGGTGCCAA AGACCATTCT TGCTCATCCG AATTTGTTTT CCTATCCTCC 540 GCAGAAATGG AACTCTAAGT TTTAGCTATT TTAATGGCCA CCCATAACAC TGTACTTCCA 600 CACCTGCCCT GTGCAATTCT GATGAAAGGG AGGTGTCACG TGGCAGTTTT TGGAAGCCTT 660 CCTTAAAAAG CTGGGCACAC AACATTAGCC CTCCGTCACC TGCCACCTGC AGTGTGTGGG 720 TGGTGACTGT ACTGAAGTGA CCTCTTGCAC CAGGCAGGCC ATGGCCAAAT CCAGGTGGTG 780 GTAGAGCAGA AAGGTAGAAG GAGCTTGAGT ACCTGAAGGC TAAGTGGGGT GGGGCCAGGC 840 TACCAGGCTA GGACTGCGCA CCCTGGTAAT TTTACGCAAC AGAAAAAAAT TGTATCCTCT 900 TAGAGCCACT GTTACTTAGA GTCTCTATTA CAGACAAACC CAATTCTGGC TTTTATAAAT 960 AATATTTTAA AAATAAAACC CATGCTCTCT ATAACCAAAG ATTTCTTATA CTGAAGATAC 1020 TCAAAAGAAC ATGAAATTTA AAAACAGGTA ATAAGGCCGG GCACAGTGGC TCACGCCTGT 1080 AATCCCAGCA CTTTGTGAGG CCGAGGCAGG TGGGTCACCT GTGGTCGGGA GTTCAAGACC 1140 ACCCTGGCCA ACATGGTGAA ACCCCTTCTT TACTAAAAAT ACAAAAAAAA AACCCAAAAT 1200 TAGCTGGGCA TGTTGGCAGG TGCCTGTAAT CCCAGCTACA AAAGAGGCTG AGGCAGGAGA 1260 ATTGCTTGAA CCTGGGAGGC AGAGGTTGCA GTGAGCCGAG ATTGCACCAC TGCACTCTAG 1320 CCCAGGTGAC AGAGTGAGAC TCTGTCTCAA AAAAAAAAAA AAAAAAACGT AATAGAGAAA 1380 AAGAATGGGC CATGGACTTC GGGGGCTTTT CTAAAATAGG CATGCCACAG ATCTCCAGCA 1440 CTGAATAAGC AAAGAGATTC CCAAGGTGCC CACTTAGGAC AGTATTCACT TGCATGATTA 1500 GCTTTAGGGG TTTTCTGAAT CTATTGAGTC ATTTTCTGAA TCATTACATT ACTGTCAAAT 1560 AAACATAGGA AGTCTACATG AGATAAGGAC TTAGCATAGT TGTATCATGT CATACCATGC 1620 ACAGGAATAT CCACATACCT TCTGAAGAAT TCAAACACAC ACACACGCAC AGCAGAAGGC 1680 AGCTAGAAAA TGCCTGCTTA TGATAAACTA GAAAAGCAAA GTGTAAAACA AAAACACGCC 1740 TCGAGACTTA 1750
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