Tag | Content |
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EnhancerAtlas ID | HS091-19977 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr17:43039110-43040880 |
Target genes | Number: 21 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Znf423 | MA0116.1 | chr17:43040340-43040355 | GGAACCCAGGGGTCC | + | 6.84 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 43039327 | 43039818 | chr17 | 43040147 | 43040263 |
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Enhancer Sequence | GGGCGCGGTG GCGGGCGCCT GTAGTCCCAG CTACTGGGGA GGCTGAGGCA GGAGAATGGC 60 GTGAACCCGG GAAGCGGAGC TTGCAGTGAG CCGAGATTGC GCCACTGCAG TCCGCAGTCC 120 GGCCTGGGCG ACAGAGCGAG ACTCCGTCTC AAAAAAAAAA AAAAAAAAAG AGAGAGAGAG 180 AGAGAGAGAG AGATTGTGTG GTGGTGAACG AATGATCTAC AGACATTCAG CTAACAGGTA 240 TGGAAACATA AGTCCTGAGT TTGAGGATCG GGGCCTCTCC AGGGTATCCT GGGTAGAGAC 300 ATGGAAGAGA AGCGCCCTCT CCAGGACTGT GGCTTGTGGT GTGGGGAGGC TGCACTGAGT 360 GGAGTTCTCT CAGCCAGGTT TCTCCACGGC CCCTCTCTAT CCTGTCCCTT CACTGAAGGC 420 AGCTTACCAT CCCAACTCCC AGGGCTGAAG TCTGGGTAGA ACCAAGCCAA ATTAGGGGAG 480 GGGCCCATCC TCTCTCCTGG GCTGGAGGCA GCACTGCAGG TCAGCTGTGC CAGAGCTGCT 540 GACTCAGCCG CGATGCTGCA ATGAAGAGGA CCCGACATAT TTGCATGAGG GCCTCCCTTT 600 AAAGCCCTTC TCCAGCCCCT TCTTTTCCCT CAACCTCTTC TTCCCAACCT GAGAAGAAAC 660 TCTTTGTGTG CTTAGCTGGG AAAACTGGTC TAGTTAAAGG TGGGAGGGAA TAAATGAAGG 720 GGGAGATGCT GTCTGCCAAG GAGCTCAGTT TCTCTGTCTA GAAAATGGAT GAGAAGACTT 780 TGCCTCACCA CTGCCACCTC TGTAAAAGTC TTTTGATGAT AAAGAAAAAA AAACATTAGA 840 TCTTGATGGG GCTTTGAGTT ATTAGGGAAG AGCTGAAAGC AAACAGCCAA CTTCTGTATT 900 GTTCCCTGAG CCCTAATCCT GGTAATATTT ATTATTACAC ATGCATTTCA TTATCTTTGC 960 TAATAAATTA CTACTAATAA CAATTATTTT TATTGCCCAG ATTAATTTAG CCTTAACTCA 1020 TTAAAACAGT GTGCTCCTTA ATAGCCAAAT CCATTGGAAC AGAGTCATCT GTCATCAGGA 1080 ATCTCCTGGT GATGTGACTG CATCAGAACT GTTATGCTTA TGTTTATTAT TTATTCATCA 1140 CCATGATTGT TGCCGTAATT ATCCTAATTA TCCATGGAGG CAGAGAGAAT TTATGCCCTT 1200 CCATCCTTAG ATGGTGGGGG ATCCAAGAAT GGAACCCAGG GGTCCCAATT CTCTGCCTGA 1260 CTGGAGACAG TTGAGGCCTG CAGCTCCTCC TGGGGTCCAA GGGGAAGTGT GGGGAAATGA 1320 GGTTGCCAAG GAAGCAGGAA AGCAGGTTTG GGCCTTGTTA TGAGGGAGCG CTGTATAATC 1380 AGCTCCTCAA GGGCTGCCAG GAGGGGAAAC TGAGGCAATG GTCTGACCAA GGGAACTGGG 1440 TGAGAGGGCA TCCAGGAAAC ACGTTCCTGC CCTCAGATCA ATGCTGGGGT CTTGGGTGTA 1500 CAGATGTGGC TCCCATAGGG GAGCCAGCCT GGCCCATGGG GGACACTTGC ATTTTCATAC 1560 ATACATTAAC TGCATTCCCA CTGTGCCAGG CACTGTGCTC TGTGTTGTGA AAGGTATTAG 1620 GGGCCAGAAA GGATAGCCAG GGGGCCATCT GCCACCACCA GGGGAGAGGC TGATCTCCTT 1680 AGGTCTTTTT TCTTTTTTGA GACAGAGTCT TGCTCTGTCA CCCAGGATGG AGTGCAGTGG 1740 TGCGATCTTG GCTCACTGCA ACTTCCACTT 1770
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