Tag | Content |
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EnhancerAtlas ID | HS091-43921 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr7:64771680-64773980 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr7:64772850-64772869 | TGCTGCCACCTACTGGGGA | - | 6.41 |
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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 |
GH07I065307 | chr7 | 64772741 | 64772930 |
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Enhancer Sequence | GTCTCCATAG AACATGCCCA TTCTTCCAGT AAAGAAATCT CATCCATGCA AGTACAAATT 60 CATGCAAGAT ATAAGGGTGA TCAGTGATAC TGTAGAAGAC ACCCACCCCA CTGGGGCCAA 120 TCAATACACT ATTTTTATCT TCCTGTCCAG AGACCATGAA TGGTTTAGAG TATTAGATTT 180 GAAGGATGCT TTCTTTTGCA TACCAGCGAA TGCAGAAAGC CAATTATTGT TTGAGTGGAC 240 AGACCCTGAA ACAGCCACAC AATTTCAATA TTGTTGGACA GTGCTTCCTC AAGGGTTTAA 300 AAATTCCCCA ACTGTATTTG GGGAAGCACT GGCTCAGAAC TTAAGAGACT TACAATTGGA 360 AAATGGGGTA CTGCTACGGT ATGCGGATGA TTTGCTAATC TCCAGCTCCT TGAAGCAAGA 420 ATGTCAGGAT AACACTGTAA AAACTAAACC ATTTGGCAGC CTGTGGGTAC AAGGTCTTAA 480 GCAAAAGGGC ACAGGGGTAC AGATATGCAA ACAAACTATG GGATACCTAA GATTTCTGTT 540 ACAGAGAAAC CAGAGCCCTG ACGGTGGAGA GGCAAAATGC AGTTGCCTCT ATCATGACAC 600 CCACAACCAG AAAGCAGCTA AGGGGCTTCC TGGGAAGGGC AGGGTTCTGC AGAATCTGGA 660 TTTCCAATTA TGGCTGAAGG TAAAGCTGCT ATATGAAGTG ATAAAAGGGG CCAACCACAA 720 CCCCTTTAAA TGAGAGCTGT AACACCAGAA TGCGTTTAAA CAATTAAAGC TTAAGATGAC 780 ATCTACCCCA TCTCTGAGGC TGCCAAATCC TCATAAACCC TTGCAACTTT ACGTGCATGA 840 AAGACTGGGT CTGGCACTCG GGATCCTAAC ACAAAAACTA AAAGAAATAT TGCAACCAGT 900 GGCTTATTTC TCAAAAGGAT TGATACAGTG GCAATGGGCT GGCCCCCTTG TCTCAAAGCA 960 GTAGCTGCCG CCTGCTTGTT GCTCAAGGGA GCTGAGAAGC TGACTTTGGG TCAGCCCATC 1020 GTGATTTATG TGCCCCATCA AGCCTGGTGT TATTTGAGCA GAAGGGTGGC TACTGGCTGA 1080 CGGTTGTCAG ATTAGGCTGA TATCGGGCCA TCCTGCTTGA TAATCCCGCA GTAAAACTGC 1140 AGACCAGTGG AGCCTCAAAC CCTGCCATTT TGCTGCCACC TACTGGGGAA CAAAGGAACT 1200 AGTACACAAC TGCCTAGAGG TTATAATCAA GTATTTTCTG GTCTCCCAGA TCTAAAGGAT 1260 GCAGCCCTCC CCTATGTAGA CTGGTTGCTG TTCATGGATG GAAGCAGCTT AGTCACCAAC 1320 AAAGGAGAAA TGCTGCCTAT GCTGTAGTAA CTCTCTTGGA GGTAATAGAG GCAAGAACAC 1380 TCCCGACAGG GACTTCTGCG GAAAAGGCTG AGTTAGTCGC TTTTACCAGA GCCTTGCAAC 1440 TGTCCCAAGG TGAGAGCACC AATATCTACA CTGATTCCAA ATATTCCTTC ATGATAGTTC 1500 ATGCACACAG AGCTATTTGG AAGGAAAGGG GACTGCTAAA AGCTGATAAT ACTGAAATTT 1560 AATATGCTAA GCAAGTGTTG GAGCTGTTGG AAGCAGTAAC AGCGTCAAGA AAAATAGCTG 1620 CTATGCATTG TCCAGGCCAT AAGAGCAGCG ATTTCAAACC AGCTAGGGGG AACACCTTCA 1680 CCTACTGCAC AGCCAGGCAT CTAGCCAGCA CCAGTGCCAA GGTCCAGGCA CCTTTGATTT 1740 CCCAAGTAGA TTTGGCAGCT TTCAAACCCC AGTGTAGTTT GAGGATGAAA AGATTGCCAA 1800 GGACAAAGGG TTTATTTAAG ACAAGAAAGG CTGGAAAGTA AATAACAAGG GCCTGGTTTG 1860 GGTGCCAGCA CACCTTCCTT CAACCCAATG CTAAAATATA TTCATGATAG CATGCATTTT 1920 GGATGAGATG CCTCGTTAAC TTTTGTGCAA AAATATAGGA AGGAAAAGGC TCACTTAAGA 1980 AGTATAATAC AACATTGCTA CCTTTGCGCT GAAAATGAGA CCAATAACTA TAGCAAAGGA 2040 CAACCCAGAC AACAGGTGAG AGGGAAGCAT CTACTAGAAA ATTGGCAGAT TGACTTTGCT 2100 CAAATGCCAC TTGCCCCTGG AAGGTACAAA TACCTCTTAG TTGTAGTGGA CACTCTCAGG 2160 CTGGGTGGAA GCCTACCCAT ATCATACCGA GTGGCCAACA GAGGTAGTTA AAGTGCAGCT 2220 AAAGAACATC ATACCCCGAT ATGGGCTCCC TGACATTATC CATAGTGACA ATGGGCCTTC 2280 ATTTACCTCG GAAATAACCC 2300
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