Tag | Content |
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EnhancerAtlas ID | HS091-22003 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr18:19314480-19316280 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXA1 | MA0148.4 | chr18:19315697-19315713 | CACAGTGTAAACAAAG | + | 6 | RELA | MA0107.1 | chr18:19315340-19315350 | GGAAATTCCC | - | 6.02 | TP63 | MA0525.2 | chr18:19314849-19314867 | GACATGTTATAACAAGTC | - | 6.7 | TP63 | MA0525.2 | chr18:19314849-19314867 | GACATGTTATAACAAGTC | + | 7.18 |
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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 |
GH18I021735 | chr18 | 19315071 | 19316448 |
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Enhancer Sequence | TCTTTCTCTT TCTCTCTTTC TTTCTTTCTC ACAGAGGCTT GCTCTGTCAC CCAGGCTGGA 60 GTGCAGTGGC ACGATCTCAG CTCACTGCAA CCTTTACCTC TCTGGTTCAA GTGATTCTTT 120 TGCCTCAGCC TCCCGAGTAG CTGGGACTAC AAGCGCATGC CACCACGCCT GGCTAATTTT 180 TGTATTTTTA GTAGAGACAG GGTTTCACCA TGTTGACCAG GCTGGCCTCG AACTCCTGAC 240 CTCAAATGAT CCATCCGCCT CGGCCTCCCA CAGTGCTGGG ATTACAGGCA TGAGCCACCG 300 CTCCCAGCCA GGGACTCTTT TCAAACTAAT GTCTTATCCT TCTTAGTGCT TCAAACTAGA 360 TCCTGTTCAG ACATGTTATA ACAAGTCAAT AGGAGTTAAT TTTGGTACAC AAAAAATGGA 420 ACTCCATGCA GTTTTTTCAT AATACACATT TTCCATGAAC ATTTTCAAGT CTCCTTGTGT 480 ATTTTCTTTC CTTTTGGGTA AGTACTGAAG AGTGGAATGG CTGGATCATA TGGCAGTGTA 540 TGATTAAGTG TTGATTTTAA GAACTTGCTG GCTGGCAAGG TGGCCAAATA GGAACAGCTC 600 CCGTCTGCAG CTCCCAGCGA GATGGATGCA GAAGGCAGGT GATTTCTGCA TTTCCAACTG 660 AGGTACCTGG TTCATCTCAC TGGGACTGGT TGGACAGTGG GTGCAGCCCA CGGAGGGCAT 720 TGTCTCACTC AGGAAGCACA AGGGGTCAGT GGATCTCCCT CCCCAAGCCA AGGGAAGCTG 780 TGAGAGACTG TACTGGGAGG AACGGGGTAC TCCGGATCAG ATACTGTGCT TTTCCCACAG 840 TCTTCACAAC CAGCAGACCA GGAAATTCCC TCCGGTGCCT ACGCCACCAG GGCCCTGGGT 900 TTCAAGCACA AAACTGGGTG GTCATTTGGG CAGATACTGA GCTAGCTGCA AGGGTTTTTT 960 TTTTTTTTCA TACCCCGGTG GCATCTGGAA CACCAGCAAG ACAGAACCGT TCACTCGCCT 1020 GGAAAGGGGG CTGAAGCCAG TGAGCCAAGT GGTCTGGCTC AGCGGGTCCC ATCCCCACAG 1080 AGCCCAGCAA GCTAAGATCC ACTGGCTTGA AATTCTCGCT GCTAGCACAG CAGTCTGAGG 1140 TTGACCTGAG ATGCTCAAGC TTGGTCGGGG GGAGGGGCAT CCGCCATTGC TGAGGCTTGC 1200 GTAGGCAGTT TTACTCTCAC AGTGTAAACA AAGCTGCCGG AAGTTCGAAC TGGGTGGAGG 1260 CCCTCTGCAA CTCAGCAATG ACACTGCAGC CAGACTGCCT CTCTAGATTC CTCCTCTCTG 1320 GGCAGGGCAT CTCTGAAAAA AAGGCAGCAG CCCCAGTCAG GCACTTATAG ATAAAACCCC 1380 CACCTCCCTG GGACAGAGTA TCTGGGGGAA GGGGCAGTTG TGGGTACAGC TTCAGCTTAC 1440 TTAAACGTCC CTGTCTGACA CCTGTGAAGA GAGCAGTGGA TCTCCCAGCA CAGCGTTCGA 1500 GCTCTGATAA GGGACAGACT GCTTCCTCAA GTGGGTCCTT GACCCCCATG TATCCTAACA 1560 GGGAGACACC TCCCAGTAGG GGCCGACAGA CACCTCATAC AGGAGAGCAC TGGCTGGCAT 1620 CTGGCAGGTG CCCCTCTGGG ATGGAGCTTC CAGAGGAAGG AACAGACAGC AATCTTTGCT 1680 GTTCTGCAGC CTCTGCTGGT GATACCCAGG CAAACAGGGT ATGGAGTGGA CCTCCAGCAA 1740 ATGCCAGCAG ACCTGCAGCA GAGGTTCCTG ACTGTTAGAA GGAAAACTAA CAAACAGAAA 1800
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