Tag | Content |
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EnhancerAtlas ID | HS047-22691 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr22:32310950-32312060 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr22:32311370-32311391 | TGAGGAGGATGGGGTGGGGAA | + | 6.82 | ZNF263 | MA0528.1 | chr22:32311373-32311394 | GGAGGATGGGGTGGGGAAGGG | + | 7.05 |
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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 |
GH22I031915 | chr22 | 32311350 | 32312067 |
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Enhancer Sequence | AGAAAGAAAT TGGCCAGGTG CAGTGGCTCA CGCCTGTAAT CCCAGCACTT TTGGAGGCTG 60 AGGCAGGTGG ATCACTTGAG GTCAGGAGTT CGAGACCACC CTGGCCAACA TGGTGAAACC 120 CCATCTCTAT CTACTAAAAA TACAAAAAAA AAAAAAAAAT TAGCCAAGCA TAGTGGTGGG 180 TGCCTGTAAT CCCAGCTACT CGGGAGGCTG AGGCAGGAGA ATCACTTGAA CTCGGGAGGG 240 GGAGTTTGCA GTGAGCCAAG ATCGTACCTC CGCACTCCAG CCTGGGTGAC AGAGCGAGAC 300 TTGGTCTCAA GAAAAAAAGA AATAGAGGAG GGGGCTTCAG TCTGTGTAGG GGAGCTGGGG 360 AAGACTGGAG AAAGGGGCAT TTGGGCTGGG ACTTGACAGC TACATAAGAG TTCTAGCAGG 420 TGAGGAGGAT GGGGTGGGGA AGGGGATGCT GGAGGGCTGG GGGGTTTTGG CAACAGAACA 480 GTCAGGAGAA GACGACTAAA AACTGAAAGG AAGAACTGCA GAGAGAGTTC CCCGACCTGC 540 CTCACCCAGC CTGCCCTTTC AACAACTAGA GGTGAGTGCT GGCAAGTCCC TGGGTGCACA 600 CTGGAGCCAA AAAATGGCCC ATTGTCTGGA AGCCCTGAGC CAGCCTGTCC CCTGGTGTCA 660 TGCCACACAA GGCCTTGCTC ACCTGTCAGC CTTTGCTCTT CCTGGCCCCA GATGTAGGTA 720 GAACAATGGC CTCTGAACAC ACCCAAGCTC CACGGTGGTA GCCGGTGTCT GATAAGACAA 780 GTAGGGAAAT GATCTCTTTC ATGTTCCCTT TCTCCTCAGA ATCAGAACGC TGCGCCCAGG 840 TTCAACCTGC TGTTTCTTCA CCAGGTGACC CTGCATAGGC TTTTGAAACC ACCCTGACCC 900 TCATCCGTCT AGCGACAAGA TGGGAATCAT CAAGACTTCG TTACGTAACT CAAGAAGTCG 960 GTGTGAGAAC CTGGGAGATA AGGGTTGTTG AGCTGGGCGC AATGGCTCAT GCCTGTAATT 1020 CCAGCACTTT AGGAGGCCAA AGCAGGCAGA TCACTTGAGG CCAGGAATTC GAGACTAGCC 1080 TGGCCATCAT GGCAAAACCC CGTCTCTACT 1110
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