Tag | Content |
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EnhancerAtlas ID | HS091-13768 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr14:77792230-77793180 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MAX | MA0058.3 | chr14:77793001-77793011 | AGCACGTGGT | - | 6.02 | ZNF263 | MA0528.1 | chr14:77792384-77792405 | TCCTCCTCCCCTCATTCCTTT | - | 6.15 |
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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 | AATATAGGTG CTGTCTGTAC GGCCTGTGTG CTTTGGCCTT CCCTCCTCCA GGTGTCTCCT 60 CCAGCCCCAA ACACTGTCAC TCCCCAGACT GGAGCTGACC AACACTAGGA GGAGCCTGGT 120 ATTGCCCAGG CTCTCCACAC CATGACATGT CTGGTCCTCC TCCCCTCATT CCTTTGCCCT 180 TCCCTGAGAT TGGCCATCAC CATACTTGAA TGCCCAAGTG TGTGTAATAC ACACATGCAT 240 GCACACGCAC GCAGTCTTCT CCACTAGTGT TGACCCACCC AAGTTTTTTT TACCCTCAGC 300 TTGCCAGGGG AAATTATCAA AAGGGATGGA GAGGAAATCT GGTGACTGGA GTCACGGCAA 360 ATGCTCTGAG GCCACCAAAG AGCCTGATGC CTGTCTAGAA TCTCTAGTAA ACAGCCCTGA 420 GAACAGAGAG AATAGATTGG AAGAGATTCT TCTCCAACAG AACAAGAGTG CCATCTGTCT 480 GTGTGTGCTG TGTGTGGCCA CCTGAGCTCC TTCCCTTGGC CCTTAGTTGC CTTCTTGAGG 540 GAGTAATTGC ATGTCTTCAA CCAAGACACT GGTCACCACT GTTTAAGGCC CTGGGGGGGC 600 AGAGTTAAAC ACAACACAGC CTTGCTGAAC TCCAGGAGCC CACAGAGTGC CAGGGCATAC 660 ACCTTTATCA CCATCCAGGG GGCATGAGGG CCCCATTGGG GGGGTCCAGA TCTTGAGGTC 720 TCTAAGAGTT CAGGGGTGAG TGAGGCAGAG CATCGTGCAT CTGGGGTAGG GAGCACGTGG 780 TGACAAGGAA AGCTGAGAGA AGGGGATAGT GCCACGGTGA GCCTTGACCA CCCAGAAGTG 840 TTAGAGAAGC CTCCCCCTCT TTGGCCTTAA TGTCACCTTA GAAGGGCTCT TTCCTTTAAG 900 AGTACGGCGA GAGGCTGTTC TTTGACTCCG CTATGTGCGG TCTCTCCTAG 950
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