Tag | Content |
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EnhancerAtlas ID | HS091-17514 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr16:57552650-57554450 |
Target genes | Number: 16 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr16:57553844-57553863 | CTGCGCCCTCTGGTGGCCA | - | 8.32 |
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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: 2 | ID | Chromosome | Start | End |
GH16I057519 | chr16 | 57553761 | 57553930 | GH16I057520 | chr16 | 57554001 | 57554110 |
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Enhancer Sequence | GAGCTGCAGG GATAAGGCCC CACCTGGTCA TGAGAACCAC CAGGATATAG CCTGGAACCA 60 CCTCCGGGGG TGGGCGCCAG TGCAGGAGTG CTCAGCGTGG AGCCAAGGCA GCGCCCAAAT 120 GGGGCAGGCA CCAGGTATTC CAAACAGACC TCGAATCTGA CCACTTCTGC TCCTCCCAAT 180 GTCTCTCCTC CTCATTACTG TCTAGCCTCC CAGTGTCTAC TCCTGGCCCT TCTCTGTCAA 240 CCCGTTTTCT ACAACAGCAG CCCAGAGGGA GCTTTTAACA AAGATGAATG CAATCATACC 300 ACCCTCCTCC CACAAAGCCT CTGATGGCTC CCAGGTGCCT TAGGGTAAAG TCCAACTCCT 360 CTCTACGCTC TCACAAAGCC CTGCACGATT GGACACCTAC CCGCCGCTCC CCCTTAGTTC 420 ACTGTACTCC AGGCACCAGG GACTCCTTTC TGTTCCTCAG ACACACCAAG TTCCTGCCCA 480 CCACAGGGCC TTTGCACATG CGTGGATCTT TCTGAGACAC TTCTTAGGAC TGATTTTTCT 540 TATTCTCAGG CCTTGACCTA AAGGCCCCCT CCTTAGGAAT GCCTCTTCTG CCCACCTGGC 600 CTGGAGGAGG GGCCTCCTCA TCCCACTCCC CACTGGAAAG CTAGCCTGGG AGGACGGGGA 660 GCTTGTGCGT CTGTCCACCT TTGTGTCGTT GTATGGCCTG GGCACAGGGC CGCCCTCAGT 720 GTACAGTGAC TAATTCCAAC ACTGCTCTGC ACACAGGTGC ATCGGCATTG CTTGGCGTGC 780 ATTTAAGACA ATAACATTTC TTGCGGTATA CAGCAAACCC CAACAAACTG CTGCTCCCTG 840 TAACACACGG ATGAGTTTTC AACACATAAT GTTGAGGGAG AGACACCAGA TACAAAAGAG 900 AACCTTTATA ATTTTCTACT AAATTGTACA TTTGTGTTTC ATTCGCTTTT CTTCGAATGA 960 TTATACTTCA TAATTTGAAA AGACTAAAAG AACAGGGTCC TGGACCCAGC CCTGAAAGGT 1020 GCTGATTCAG GAGGGTGGAG GCGAGGTCTG GGAATCTGTA TTTTAGGAGA TTTCCTCAGA 1080 GATTCTCATG TAAGACCAGT CTTGGTCCCC TCCAGGACAG TTTCAGGCTC TAAAGTTCTG 1140 TGATCCTCCC AGCTGCTAGA AACCCACCGA TCCAGTGTGG CGTTCCCTGG GTGGCTGCGC 1200 CCTCTGGTGG CCATTGAGGC CTGCACAGGA GGCCGTAGTG GCAGCTCAGC CTGCTCTGAG 1260 CCCCCACACT GCAGTGGTGG ATTCCCTTCT CTGGAGCCTC AGTTTCCCTA TCTGTAAGAT 1320 GGGGACATGA GGACCCAGCT CCCTGGGCTG CCATGAGGCT TCAGTGACAC CTAGTACAGA 1380 TAGGAACCCA ATGAATGCCA CATCCAGCCT CCTCGTCTTC ATCCTGGTCT ACAAGGCCCC 1440 CTCCTGCGGC CTCGCCTCTC ACTTCCTGCT CTCCAGCCAC CTGGCCCTCC CTGTTTCCCG 1500 CACACGCTGG GCTTGTTCCT GCCTCAGGAC CTTTGCACCG CTGTGCCTTC TGCCAGGAAC 1560 ACTCTCCCCT GTATCTTTTC AAGGACAGCT TCCTCTAGCC CCTTTAGGTC TTGCCTCAAA 1620 TGCCACCTTC TTAGGCCTTC CCTGACCTAC CACCCCATCT CTCTCATTCT GTTTTGACTC 1680 CTTCATAAAT TATGAATCTG CCTGGTGACT GTCGGTCTCC CATGCCCACA GCCCCCACAA 1740 AGTGAGCTCC TGAAGGCAGG GACCTTGCCT GCCCAGCACT CAGAACAACT CAGAAAAAAT 1800
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