Tag | Content |
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EnhancerAtlas ID | HS091-32711 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr22:24999500-25001000 |
Target genes | Number: 26 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXH1 | MA0479.1 | chr22:24999829-24999840 | TGTGGATTGGG | - | 6.14 |
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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 | AGAGCCCTGG GTTCTTTATC CGACTGGGTC TGGGCTGGGG GCCTCTGTTT CTTGGCTGAT 60 GAGTTTATGT GAGTTTGAGT GAGGTATGCG AGTGGGTGAA GGAGGGCTGG GGGGAGTCAC 120 CTGACTTGTG CGAAGAAGCT CTTGAGAGAG CCGTGGCTTC TTGGAATTAA GAGGAAAGAG 180 TGCAGCATGA ACAGACAGGC CCTGGAGGAT CTGGCAGCCC TGAGTGGGGG CGGGGGGTCA 240 GCTCTGGAGT AGAGCCAGAG CTGTGATGGG GTTGGGGGAC CCTGTGTCCT TGGGCCATGC 300 TTGCCTCGCT CCTGGGTTCT GTTTGTGGCT GTGGATTGGG GTGGGGCAGG GCCGGTTGTG 360 CGAGGGGTCA TTGCCCAACT CCAGGGGGCG CCTGCCACCT CTCAGCTATA TATATAGGGA 420 TATATATAGT TCTTTCGACA GGTTTCCAGC AGGTAGTGGT TATTAAATCT TACTGAAGGG 480 GTGTTTTTTC TGATTCTCGG CTCTGTGCCG CAAGGGTGGA AACTGTGAGA GACAGATTCC 540 AACTCCACGT CTGGGTAGTA AGCATCCAGT CCAGGGCTGT AGGCAGTCCT GGGGAAGACG 600 CCAGAGATCT GTGCATTCTC ATATCGAGGG ATAGCGACTC CAGGCTGGGG GCTGGCAGGG 660 TAAGGGGTGG GTGGGTCCTG GGCTTACCCG CAGGTCTGCA GACTTCCTGG GGCCAGCTGA 720 CCTCGTAAAA TCCCTTTTGT CTAAGCTTCA GTTTCCTGCC TGTGAATGGG GTTGGGGCTG 780 TGCTCTGGTT TCACCCTTGT GGCTCTGGGG TTGTGGTGAC AAAGCCATCA AGCTGGGTTG 840 AAGGATTAAC CAGGAAACTT CAGACTGGCT GCCGTGTCTA CCTCTTCCTC ATACTCCTCT 900 CTCTGCTGCA TCCTGGGAAG CTGCTCTGCT CAGCCTAAAT GAGGCTCAGT TGTGTGTGTG 960 CGCACGTGCT TGCACGTGTG TTGGAAGTGG GTGATACTGA CACCAGAGTC TGTGTCTCTG 1020 GGTGAGTGAG GCTTGCACAT TTCTCGGGAC AGGGAACTCA CTACCTTATG TGCCCAGGAC 1080 AAGAGCTGTG GGGTCTGGAG AAGACTTCTA GGCCAGCCCC TGCAGTCCTT CCTCAGGTGA 1140 CATGGCTTCC CCAGACCCAC TTCCCCCTAG GTGCCCTCTC TGCATTCAGG GGGTAGAGGG 1200 CTGACTGGGA CAGAATGTGA CACACTCAGC ATGTGAGGAA AAGCCTCCTT CATTCTGTAG 1260 GCCCTACCTC TATTAACATG TCCTTTGATA AAGTGCCTCC CCTCCTGTCT CCCCTCTCTG 1320 GAATCCTCAG CTGCTGCCAG GCTTCAGCTG TGCCCCATTG AAGGCAGCTC TGTCTCCCTA 1380 CTTTCCCCAG CCCAGGGTTT TCCTTTTGGG GTCAGCTGCA GGGATCTGGG CCATCCTTTG 1440 CCCACTCAGA CTTTCTTTCT GCCCACCTGC TGCTGTGAAT CCTGTATGTC ATATATATAT 1500
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