Tag | Content |
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EnhancerAtlas ID | HS091-42495 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr6:145953750-145955980 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr6:145955314-145955333 | TGCTGCCCCCTGCTGACAG | - | 6.24 | ZNF263 | MA0528.1 | chr6:145955867-145955888 | CCCTCCACTCACTCTTCCTCC | - | 6.87 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr6 | 145953997 | 145954295 | chr6 | 145954783 | 145955758 |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I145634 | chr6 | 145955261 | 145955410 |
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Enhancer Sequence | ATAACAGGTC TGTGACAACT AGCGGTGACA GTCAAGCCTA ACAAACTGTC TTCTTTCTCA 60 GACTTCAACT GAGAGCATTA TGCTGCAGCT CAAAACACTT CCAACTGGGT TTTTCTCTAG 120 AGTTCTAAAA ATATTCAGCT GATTAATCTA TGTGTTCATT GGGCTAATAC TGTGAGCCAC 180 AGACATTGGT CTATTGGTAA AAAGTTCCCC TGCCACTCAG AAGTGGTTAT TAACCCTTAG 240 ATTACACCCC CAGGTTAGGC CAAGCCAAAG AAATCCATTA GTCGGTCTTA CAGCTGGGCC 300 TTTATCACGT GGAAGCTTGC ATTTTGCAGC TCAAATGCCA CTGCACTGTC TCAGCCTGAA 360 AGAAGCTATG CTACTGCACT AACAGTTACG ACTGTGACCT GGTAACCCAC TGACCGCAAA 420 AAAGGTTCGT GAACACAACT ACAATGGGTC CTTGGGGATA CAGTTTTCCC TCAGGCTTCT 480 GCAGAGTCCC AAACTATCAA GCAAATTACT ATCTGTCAGC AGAGCCTTCA GGTAATCAGT 540 GTGTGGGTTG GGATGGGATG GCGGGGGATG CGTGGCACAG TTGGCAGCCT AACTTCTCCC 600 AGCCTCGTCT CACATCATTC TCCAACAGGA TAACAATGCT GTCAAATCAG ATTCAGAGAT 660 GCTAACATCA AAATGCTCTC TGGAAGCTAC AGTCCTTCAA ATCCTAACTA TCTTCTCTGT 720 TTTGAAACCA GGAAAACCAG CTGGACAAGG TAAATATCAC CTGGATTCAA CCAATGTGCA 780 TCTTCGCAAA TGAAGTTTTT CTTTTTTTCT TCCTTGAAGA AGGGCAGAGC TCTTACAGCT 840 AAATCATGCT TCCTTAGGTC AGGTTACCAA GAGGAATAAC CAGACTGTCA GCAGCTCTCT 900 CCACCTTCAG GAACAAACAT TATACCCCAT CCCCAATGGC AATTCAGCTC AGACACAGAT 960 CAACAAAGGG GCCCAGCCTG GCCAGGAGGA CCACCTGAGA TCCATAAAGG GCTGAGGTGG 1020 GCAAGGTCCA GAAACGTAGA TTTCCTGTGG TCCTCATGGT TTTTTATCTT GCAGACCATT 1080 CACTCTTGGG GAGACAAGCT ACTTCCCTTG CAATTTGTAG GCTCTGCCTA ACTCCAGATG 1140 ATCATGAACA TAAGGGGTTG AAATTGCATG GGTCTGAAGA ACCTGCCTGA AGCGTCTGTG 1200 TAAGAATGCA GGGAGAAGCT TCATAGCTGG TAAAGTTGCT GTCTGGAGCA ATGTTCTGGG 1260 TCCGACTGCC AGCCTTGAAA TTCAGAATGG GCCTCTTTTT AGTTCTATGA CATGGGCAAT 1320 AACTTTTTCA TGCCTCAGCC TCTTCGTCTG CAAAATAGAG ACAGCTACAA TATCTGCCTG 1380 GAGTCTTATT ATGAGAATTA AATAAGCTAA TTCTTGTAAA TTGCTTAGGA GAGTGTTTTG 1440 TACATAATAT ACATTTGGGG GAAGAGGGCT AAAGATAGAA ACGTCTCTGA GCTGGATATC 1500 ACTGTCCTTT CCCCAGCAGA GGAGGTCATC AAACTCCTTA GCCTCTCCCA TTTCTGAAGC 1560 TCTCTGCTGC CCCCTGCTGA CAGCTGCTTG ATACTATCGG TGTAACTTGG TTCTCTCCTC 1620 TGCCGACTGT AGTTATCTCT ACTCCTCTTC GACAAGTACC CTATTCTACA ACCAGGCTAA 1680 AATCCCTATC ATTCCTCTAA AATTCCATGC TTCTGTGCCA TAGCCTGTGC TGCTGCTTCC 1740 CCCTAGCATG CCCTTTCTCC CTCCACATCT ACCTATCAAA GCCATGCCCA CCTCAAGTGC 1800 CATGGCATTC ACGCAGCCTC CCTTTGTCGC TCCCCAGAAT GTGCTCTTCC CATGCATAAC 1860 CCTCCTCCAG CACGGTCCTC ACTCCTCTCT TACCCATTCC CCTCTGTGCT GTAATTAGTG 1920 TCGAACTCGT CTTACTGTAC AACTGCTTCT TCCTGCTATA GGATAGCGTC TAAAGTCCTT 1980 TTTGTCGCTC AAATCCTGCA GGATCATCTT TCCTCGTTCT CTGATCCAAG CCACATTGGT 2040 CTTTCAGTTT TTGCAACACT CTGTGCTCTC TCCTGCCACA AGGATTCTTC TAAGCTGCTG 2100 CTTCTGCCTG GGTCACTCCC TCCACTCACT CTTCCTCCAG CCCACCCTCA GATCTTAGCC 2160 CAAACACTAC TTTCCAAGAA AACCCTCTTT GACCCCACTT CTTGGCCTGA TTACCTGTAC 2220 ATAATCTCAT 2230
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