Tag | Content |
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EnhancerAtlas ID | HS118-15732 | Organism | Homo sapiens | Tissue/cell | Liver | Coordinate | chr6:1321980-1323620 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXA1 | MA0148.4 | chr6:1323160-1323176 | CTTTGTTTATTTAAGA | - | 6.26 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH06I001321 | chr6 | 1321605 | 1323610 |
| Enhancer Sequence | TCTTAATATT GTCATCAACA AATGGCCCTA ATAAGTATCT TCCAAGAGGA TCGTGATCAA 60 AAACGTAAAG ATGTAACTCT CCCTGGATTC AAGGACCTCT TTCAAATTGG CAAGGATTCT 120 GATGTAATGA AATGCTGGTG GTTGTGCAAT AGTTTCTGCA CTGTATCTGT TCGACGTTAT 180 TAAGATGGGT GGGTGATTAG AAGCACATGC TCTTCCTGTC ATTTGCCAAC TTACACACAG 240 CCTGGAAAAG AGAATTGTAT CAACCTTCAT TTTTGGTGAA CTGCAGCCAA ACATAAACAT 300 TAACATAATA CCACATTTCC CTTCCCATTC CTGGACCCTC TTTGTCACTG TTTTCAGGAA 360 CAGTTTAACT TTGAAGCCTT GCCATAATTG AACCTTTGTA TCATATCTGT TTGAAACCCA 420 AAATGCTATA CAATTCAACA TCTTTGACAT GTATTTGTTA TTTCTGATCA CCAATTTCTA 480 GCCATTAAGA AAGAAGTAGA AAAGTTTTGC AACCTTTGGC TGGCTCTACC CACTGTAGTT 540 AAATGTCTGG TCATGCTCAA AATCACAGAA GTTGCCCATT CAAAAAAAGA ACTCAGAATG 600 AAGACACTAA AGAGACCCTA GTCTAAATTC CAGCTGTGTC TCACACAGCT GGGTGACCTT 660 AGGGAAACGG GTCATCCCTG CAAGCCTCAT AAGGACGAGG GTTGGGCTGG AACATGTCTT 720 GCACACCTCC CTCACAGTTC ACACCCATGA AAACCCTCAT ATAATGTCAA AAATAACACG 780 CTAATGTGTT TTTTTTTTCC CTTTTCCCTA AACTCAATCA ACTTGAGATC AAGTGTGAAT 840 CTCAGGGACA AGTTTCAGTA TGTCATTCTT CAACATGATT AAAGTACTTA CAAACACAGC 900 AGAATATATT GGATGCCTTA GGGTACAATG GATATATACA ACTTGTCATT CTAATGGGTC 960 ATAACATGTA TTTCCAATTA TGTTTCCCCC AGTGTGCTCC TGACAACTTA AGTTTCTCAC 1020 AAAATCCCAG CTTTGAGAAT TAGAGGAGAA TGCTTACTTC ACAGGCAGGA GACAGAAGTT 1080 GGGCTATTTT CAAGAGATTT CATCATAAGC AAGGCATTTA GGGCTGGGTC GCATGGTGGC 1140 TCCCAGGCCG CTGCTCTGGG CTGACAGGAT CAGCTCAGTC CTTTGTTTAT TTAAGAACAA 1200 AGTCTAAAGG CAATTCTCAG GGTAGCAGAG TTGATATAAC CTAAAAATGC AATAGCCTGG 1260 GTGCTCCCAG CACTTTGGGA GTCCAAGGTA GGAAGATCAT TTGAGACTAG CAGTTCGAGA 1320 CCAGCCTGGG CAACATAGTG AGATGTCTTC TCTACAAAAA AGTAACAAGA ACAACAAAAA 1380 ATTAGCCAGG CATGGCGGCT TGTGCTTGCA GTCCTAGCTA CTTGAGAGGC TGAGGTGGGA 1440 GGATCGTTTG AGCCTAGGAG TTCAAGATGC AGTGAGCTAT GGTGGTACCA CTGCACTCCA 1500 GCCTGGGTGA CAGAGAAAAA ACTCCTGCCT CTAAAAAAAT AAAGAAAAAT AAAGCATAAA 1560 AATATCAATG TAATTAGCAC CAAGGGCCTC AAGGCATGGG AACAAATGTA TATGTGTTCA 1620 TACAAATATA ACATGAGAAT 1640
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