Tag | Content |
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EnhancerAtlas ID | HS047-20695 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr2:241365850-241366860 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr2:241366326-241366347 | AGAGCAGGAGGAAGAGAGAGA | + | 6.78 | ZNF263 | MA0528.1 | chr2:241366332-241366353 | GGAGGAAGAGAGAGAAGGGAG | + | 6.93 |
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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 |
GH02I240426 | chr2 | 241366028 | 241367274 |
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Enhancer Sequence | ATGTCACATC ATCAAACTGA ACTTAGAAAG GGCCCCTTTT CCCAAAATGA AGAGATTCAC 60 CGCAGCCAAT CAGTCTACCT GAGTCAGGAG ACTCAGGAAG TCCCTCCGTG TTAGTCTGAC 120 AAGGAAAGTG ACCCCACAAT GCCCAATCAC TTGCTGTCCT CTTATTTCTG TTTCTTCAGC 180 CTTTTCTGCC TGTAAAGCCC ACCTCTTCCA CTCAGCTTAT GGGAACACCC TTCCTAACTC 240 TCCAAATGCG ATGCTGCCTG ATTCGTGAGT CACCAGGGAT AGCCAATTAG ATCTTGCGCG 300 AGTCGGCTCT TCCATTGCTA TGAAGAAACA CCTGAGGCTG GGTCGTTTAT AAAGAAAAGA 360 GGTTTAATCA GCTCAGGCTG TAGAGGAAGC ACAATACCAT CATCTGCTTC TGGTGAGGGC 420 TCAGGAAGCT TCCACTCATG GTGGAAGGCA AAGGGGGAGC AGGTGCGTCA ACGGCAAGAG 480 CAGGAGGAAG AGAGAGAAGG GAGAGGCCCT AGGCTCTCTT AAACAACCAG CTTTCTCGTG 540 TGAACTAACT CAGCGACAGC TCACTCATCG CCAAGGGGAT GACGTCAAGC CATTCACTAG 600 GGTCCCACCC CTGTGACCAA ACACCTCCCA CAGGGCCTCA CCTCCACCAC TGGGGATCAC 660 ATTTCAACAG GAGATTTAGA GAGAAGAAAC TTTCAAACCA TATCAGATCT TAACTAAATG 720 TGTTGAAAGT TTGTTTTGTA ACAGCACACA CATGCCTGGG TTTCCAGCTG TGTAGCAGGA 780 ACTGGTGCCT GTCCACCAGC TAAGGGATAC GTCTAAGTCA TTTTCTTTCT GCCACTTCCA 840 GGTTACTCTG CCAGGGGACC CAGGGAAACC CAGCAGGCAG CGGTCACTGG CGACCTTGAG 900 TGTGGAGAAG GGAGCGAGGA GGAGCCTGGG TGGACACCTG CAGCACCTGC TTCAGAGGCG 960 AAGTGGGTAC AGGTACTCAC TGCACTCGCC TCCCTGCACT GGGTGGGTCC 1010
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