Tag | Content |
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EnhancerAtlas ID | HS091-15935 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr16:789740-790910 |
Target genes | Number: 36 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Zfx | MA0146.2 | chr16:790519-790533 | GAGGCCCCGGCCCG | - | 6.32 |
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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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Enhancer Sequence | AGAGCAGGAA GAGACCCCAA ATCAGCCCCT GTGAGTGGGC GGAGGTTCCC TGGGAGGCCA 60 GGCCTCAAGG ATGGCTGCCC AGCCGCACAG CCTGAAGGCT CTGCCAGGAG CCATGCACTC 120 AGGGACTGAG GCTGGTCCCA CCGTCTTCTT CCTGCCCCAC TGCTCTCACC CAGGGATCGG 180 GTTCCCAACA TCCTGCGGCA CTGAAGTTCC CAGTGTGCAG GAAGGCCAGT GCTAACAGCG 240 CCTGCAAACT ACCCACCTGC GGAGACACCA CCAACACTGA CCTTCACCCT TCACGTGAAC 300 AGGGGGCGTG ACCACCACAG AGACCAGAGT TGCACTGCCC ATCGAGAGGA CGTGTGCTTG 360 GATCTGTTTG GAGACCACCT CCTGCTCAGT GCCCGGGAAA CAAGTGGATT TCTCTCTCTT 420 CTCCTTGAGA ACCCTGGCAG CCCAGAAAGC CGCCTCCCAG CTCATCCCTG CCGGAAGCGC 480 TCCCAGCAGC CCGCCTCTCG CCCTGCTCAG CTCTGGCCCC GCGGGGCTGT TGGACATGGA 540 CAGGCAGGTG CACCCAGAAA AGGGCGCCTG CAGCCTCCCG GGTTCAAGGG TAGCTGTCCG 600 GCCCACCAGG GCGACGTTAA GGACAGCTCT ACTGAGGAGC CACTGCGGGG CGTCTAGCGG 660 GCCGCCCCTA CTGCCCTCAA ATGAGGTGGG GTCCCCACCG CACCCGTTTA TGCAGATGCA 720 AAGGCTGTGG CTTGGGGGTC CTGAGGCCTG ACAAGGCGTC CTGCGCAGGG GAAGGGGAAG 780 AGGCCCCGGC CCGGGCCCCG CCGCCCTCCA GCTGCGACCC AGGGGTCGGG TTAGGGTTAG 840 GGATGTGTGG GAGCCGCCTC TGCTGCCTCC TCTGGGTTGG GCAGGCCGGC GCGAGCCCGC 900 GACCACGGGA CCCTCCCACG CAGCCCGCCC GGACACCATG GGGCACAGGA GCGGGTTGGG 960 GGGCGCCGCC CTCCCTGGCC TCAGTTTCCT TGTTGGTAAG AAGCGGGCCT CAGTGTCTGA 1020 GGCCCCGCGC CCGGGTCGAT AGAGTCCCTG ACGGCCCAGA CCGGGCTCCC GGGATTCGGA 1080 TCTCATTCCT CAGGGGAGGA AGTGGGGCGC AGAGCAATTT CCCTCCGCGC GACAGGGCAC 1140 CGAGCGCAGC CTCGACCCCG CCCGCCCAGG 1170
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