Tag | Content |
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EnhancerAtlas ID | HS088-48775 |
Organism | Homo sapiens |
Tissue/cell | HeLa-S3 |
Coordinate | chr7:94654240-94656580 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXA1 | MA0148.4 | chr7:94656180-94656196 | CTTTGTTTACACTGTG | - | 6 | Nr2f6(var.2) | MA0728.1 | chr7:94654597-94654612 | TGAACTCCTGACCTC | - | 6.22 |
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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 |
GH07I095025 | chr7 | 94655272 | 94658675 |
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Enhancer Sequence | CAAGTTTAGT GCTTCCTTCA GGAGCTCTTG TAAGGCAGGC CTGGTTGTGA GAAAATCTCT 60 CAGCCTTTGC TTGTCTGTGA AGGATTTTAT TTCTCCTTTG CGTATGAAGC TTAGTTTGGC 120 TGGGTATGAA ATTCTGGGTT GAAAATCCTT TTTTTTTTTG AGATGGAGTC TCGCTGTCAC 180 CTGGCTTGAG TGCAATGGCA TGATCTCAGC TCACTGCAAC CTCTGCCTCC TGGGTTCAAG 240 CAATTCTCCT GCCTCAGCCT CCCGAGTAGT TGAGATTACA GGTGGTCACC ACCATGTCTG 300 GCTAATTTTT GTATTTTTAG TAGAGACGGG GTTTCACCAT GTTGGCCAGG CTGTTCTTGA 360 ACTCCTGACC TCGTGATCCA CCCTCCTCAG CCTCCCAAAG TGCTGGAATT ACAGGCGTGA 420 ACCACTGTGC CTGGCGAAAA TTCTTTTCTT TAAGAATGTT GAATATTGGC CCCCACTCTC 480 TTCTGGCTTG TAGGGTTTCT GCAGAGAGAT TCACTGTTAG CCTGATGGGC TTGCCTTTGT 540 GGGTAACCCG ACATTTCTCT CTGGCTGCCC TTAACATTTT TTCCTTTATT TCAACCTTGG 600 TGAATCTGAC GATTATGTGT CTTGCAGTTG CTCTTCTTGA GGAGTAACTT TTTAGTATTC 660 TCTGTATTTC CTGAATTTAA ATGTTGGCCT GTCTTGCTAG GTTGGGCAAG TTCTCCTGGA 720 TAAAATCCTG AAGAGTGTTT TCCGACTTGG TTCCATTCCC CCTGTCACTT TCAGGTACAC 780 CAATCAACCA TAGATTTGGT CTTTTCACAT AGTCCCATAT TTCTTGGAGG CTTTATTCAT 840 TCCTTTTCAT TCCTTTTTCT CTAATATTGT CTTCATGCTT TATTTCATTA AGTTGATCTT 900 CAATCTCTTG ATACCCTTTC TTCAGTTTGA TCAATTTGGC TATTGATACT TGTGTATAAT 960 TCACGAAGTT CTTGGGCTTT GCTTTTCAGC TCCATCAGAT CATTTATGTT CTTCTCTAAA 1020 CTGGTTATTC TAGTTAGCAA ATTCCTCTGT CCTTTTATCA AGGTTCTTAG CTTCCTTGCA 1080 TTGGGTTAGA ACATGTTCCT TTAGCTCAGA GGAGTTTGTT ATTACCTGTC TTCTGAAGCC 1140 TATTTCTGTC AGTTTGTCAA ACTCATTCTC CATTCAGTTT TGTTTTCTTG CTGGCAAGGA 1200 GTTGTGATCC TTTGGAGGAA GAGGCTTTCT GGTGTTTGGA ATTTTCAGCC TTTTCATGCT 1260 GGTTTCTTCT GATCTTTGTG GATTTATTTA CCTTTGGTTT TTGATGTTGG TGACCTTCAG 1320 ATGGGGTTTC TGTGTGCACA TCCTTTTTGT TGATGTTGAT GCTATTTGTT TCTGTTTGTT 1380 AGTTTTCCTT CTAACAGTTA GGCCTCTCTA CTGCAGGTCT GCTGGAGTTT GCTGGAGGTC 1440 TACTCCAGAC CCAGTTTACC TGGGTATCAC CAGTGGAGGC TGCAGATCAG CAAAGATTGC 1500 TGCCTGTTCC TTGCTCTGGA AGCTTTGTCC TAGAGGGGCA CCCTCCAGAT GCCAGCCGGA 1560 GCTCTCCTGT GTGAGGTGTC TATTGGTCCC TGCTGTGAGG TGTTTCCCAG TCAGGAGACA 1620 CAGGTGTCAG CGACCTACTT GAGGAGGTGG TCTAGTCTGA CCCTTAGTGG AACTCAAATA 1680 CTGTGCTGGG AGATCTGCTG CTCTCTTCAG AGCTGGCAGG CAGGGACGTT TAAATCTGCT 1740 GAAGCTGCAC CCACAGTTGC CCCTTCCCTG AGGTGCTCTG TCCCAGGGAG ATGGGGGTTT 1800 TATTTATAAG CCTCTGACTG GGGTTGCTGC CTTTTTTTCA GAGATACCCT GCCCAGAATG 1860 TGGGAATCTG GAGAGGCAGT CTGGCTACAG TGGCTTTGCT GAGGTGTGGA AAGCTCTGCC 1920 CAGCTGGAAC TTCCCCTCTG CTTTGTTTAC ACTGTGAGGG GAAAACCACG TACTCAAGCC 1980 TCAGCAATGG CGGACACCCC TACCCCCACC AAGCTTGAGT GTCCCAGTTC GACTTCAGAC 2040 TGCTGTGCTG GTAGTGAGAA TTTCAAGCCA GTGGATCTTA GCTTGCTGGA CTCCATAGGG 2100 GTGGGATCTG CTGAGCTAGA CCACTTGGCT CCCTGACTTC AGCCCCCTTT CCAAGGGAGT 2160 GAATGGTTCT GTCTTGCTGG TGTTACAGGT GCCACCGGGG TATGAAAAAA TACTCCTGCA 2220 GCTAGCTTGG TGTCTGCCTA AACAGCCACC CAGTTTTGTG CTTGAAACCC AGGGCCCTGG 2280 TGGCATAGGC ACTGGAGGGA ATCTCCTGGT CTAAAGGTTG CAAAGACCGT GGGAAAAGTG 2340
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