Tag | Content |
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EnhancerAtlas ID | HS091-47055 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr8:144618620-144620170 |
Target genes | Number: 27 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF4G | MA0484.1 | chr8:144619478-144619493 | TGGGACCAAAGGCCA | + | 6.18 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr8 | 144619712 | 144619867 | chr8 | 144619962 | 144620055 |
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Enhancer Sequence | AGGCTGTGGA GACAAAATAC AGGCAGCTCT CAACAAGCCC TGGGGGTTCT GCCCACCCAC 60 CCTTCCTCAC CAGGACCCGA GGAGCGTGGG AGCAGCTCCT GAAGGCCAGG ACCAGGCCAC 120 AGCGGGTCCT TTCTGGACCC TGCCTCCCTC AGCCCATGGC GGCCCTGCCC ACCCTCCACA 180 GCCAGGCTGA GGCGGCAGGC TTGGATCCAC AATCCCAGAT GACCCCAGAA CTAGGGCAGG 240 CTGCCATGCT CCCAGGGAGA GCAGAGGGGC CTCAGTGCTC CGTCCCCACC CGCATGTCCA 300 CCCCCTCCCC ATCTGCCCAG GAAAAAGGAG CCTCTACGTG GGGCAAAGAG AAGGGCCGAC 360 ATCCCTGAGG AGAGCGGCCA CCGGCCCCAA GTGGCCTGCC AAGCCCCTCA GTAAGGGGGC 420 AGCTTCTCCA CGCTCCCTCT CCACACTTCC TGGACAGAGG GAGCTGCCAG CATGGTTTAG 480 AGCAGAGTTG CCACCGAGAA ACAGCCAGGA GTGGGAGCCG GGTGCCCATG CGCCTCAACA 540 CGGCACCTAT CTGGGGGACG AGGGCCAGAG AGAATGAGCT ACACGAGCCA GCAACCTAGA 600 CCAGACGGCA GGGCACCACT GTGTCTGATG ACAGAGGCAG GACCCCCGCC CTCTGCCCAG 660 CAGGTGCAGC CACCACCTTA GCTGCCAACC TCATGGAGTC CCTGAGCCCA GACCAAGCAC 720 TGTGCCATGA CACCATCTCT GAGTCTCATC ACAAGTCCGC AAGGGTGGAG GCCGGGAGAG 780 ATGTGCGCCA AGCAAGTGAG TGACTCTGCC TGGCTGCCTG GCCAAGGGGG CTGGGACCTA 840 ACACCAATCT GCTCGCCCTG GGACCAAAGG CCAACTGCAG CCTCAACACT CCGCAAGGGA 900 GGCCACAGAG CCCAAAGCCA GGAATGCCTA AGGAGGCTCC CGCCTACCAG CAGCCCCCGG 960 CCCCTGCCCA CTCAGACCAG CTGGAGCAGC CCTCAGCCTG AGGGCCAGCA AAGGCCAGGC 1020 CTCCTGGAGC CCAAGCCCTA GACACGGGGC ATGCAGGAAA GACCAGGCAC CCCTGGCAGG 1080 GCCCAGAGCT CTGGTCCACC TCCCAGCACA GACCCGTGGC CGGCAGGTCC AGGCCAGGGG 1140 CAGACACACT GCTCTCTGTC TCACCATCCC CCTGGGGACA CATGGACCCT GGACTGGTCC 1200 CTGGGAGCTA CTCCCCCTGC GCCTGGCCTG GCACAAAGCC TTCCCTCTGT GAACCCTGTG 1260 CAACTGGAAC GGAAGCTGCC CCCAGCGAGC TGCTTGTCTC TCACCGGCAG GAGAAAGGAT 1320 GGGCTTGCCA GCAGTGTGAG GGACGGGAAA CCTGTCCCCT AAGTTTATGC CGGCCAGGGC 1380 CCCGGCCCCA GGCAAGCCCA AACCACCACA GCAGCACTTC CTGCCTCATT TCTTGCTGGA 1440 AATGTGAACG CAACTGCAGG CAAAGCTCCG AGCTCAGCAG ATCCATTAGG GGTGCCAAAC 1500 AAACCCTCCT CACAGCCCCT CACACTCTAC CGCAGCCGGC CGGGATGCCC 1550
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