| Tag | Content |
|---|
EnhancerAtlas ID | HS118-16728 | Organism | Homo sapiens | Tissue/cell | Liver | Coordinate | chr6:150271190-150272410 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr6:150271418-150271433 | CAGGTCACAAGGTCA | + | 6.49 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ACAGTAAAAG AAATTAGCAA CACAGTTAAC AGCCTATAGA ATGGGAGCAA TATCTGCAAT 60
CTATGCATCT GGCAAAGCTC TAATATCCAG AATCTACATG GAACTTAACA AGCAAGAACA 120
AAATTGCAAT TAAAAAATAA GCAAAGAATG TGAACAGACG CTTTTCAAAA GAAGACATGC 180
AAGTGGCCAA CAAACATGAA AAAATGCTCT TTGGGAAGCC GCAGTGGGCA GGTCACAAGG 240
TCAGGAGTTT GAGACCAGCC TGACCAACAT AGTGAAACTC CGTCTCTACT AAAAATACAA 300
AAATTAGCCA GATGTGGTGG TGCATACCTG TAACCTGTAA TGGTGCATAG TCTGATGTTG 360
GAACTATGAA GTACCTTGGA CTGGTACTTT ATAGTGTTTT CCAGCAGACA GCACTGCTTA 420
TTTTTCAAAT ATTTCAATAA GTCGGGAGGG TTTGCTGACA GCGAGTTTGT GCCCTGAGCT 480
CTTTGGCACT GAGGGCAAAG AGCAGAGGGG TGTGGTCTGG TGGCCCAGCA TTTCTGCCCC 540
GGGGGAGGAT TCTCTTCTGC TGCAGTGAAA ACCAACAGGA CGCTGCTTCA TCCCAAGGGG 600
ACTAGGAAGA TAGGTCAGAG TGAGGAGCTT TCTGAGTGTT TCAGATCACA CAGTGACTGC 660
CTGCTTGATG GCTTCAGAAC TCCTTCATTA GCTGGGAGAC AGCCCCCGAG GTAAAAGGTG 720
CATGGGCACG ATGGGCTCGA CATGACAGCT TTCGAGATGA CAGGCAGTTT CTCCCGTGTG 780
TTTCTATGTG TCTTTGTGTG TGCCCGTGTA TGTGCATGGC TGTGTCTGTA TTTCTGCATG 840
CATTTATGTA TGTGTGTTTG TTTGTGTGTG TGTGTGCCTG TGTGGTGTGA GTGTGTGTGT 900
GTGACTGTGC CTGCATGTCT CTGTGTGTGT GCATGTGTGT CTGTGTGTGT GTGTGATAAC 960
ATGCATATAT GAATGGTGAA TTGATTTTCT GCTTGATTTG CTATGGAGGG AGACAGGGAC 1020
TCCAGGGGGG GTTCCTGCCC ACCCCTTGTT CCCTGTCTTC TGACATTCCC TCCTCCCTGT 1080
GGAAAGAGTC TACCCCAGTA ACTGAGGGTT CGTTAGTGCA GACGTCTCAC AGCTCTCCAA 1140
AGTTCTGTGA TATTTGTATC CCCAGGCCTC CTCCTCATGC TTGTCCATCT GCTGGATGCC 1200
CTGTCTTCTC GAGGCCACCT 1220
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