Tag | Content |
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EnhancerAtlas ID | HS047-05594 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr11:14443660-14444670 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr11:14444584-14444605 | CCCTCCAGCTCTCTCTCCTCT | - | 6.12 | ZNF263 | MA0528.1 | chr11:14443920-14443941 | CCCCCCTCCTCCCCCACCCCA | - | 6.37 | ZNF263 | MA0528.1 | chr11:14443914-14443935 | TCCTTTCCCCCCTCCTCCCCC | - | 8.18 | ZNF263 | MA0528.1 | chr11:14443911-14443932 | TTTTCCTTTCCCCCCTCCTCC | - | 8.69 |
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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 |
GH11I014421 | chr11 | 14442816 | 14446605 |
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Enhancer Sequence | AGACTGTGCC ATTGTACTTC AGCCTGGGCA ACAGAGCGAG ACTCAGTCTC AAAAAAACAA 60 AAACAAACAA AAGAAACCGA GGCTCAAAGA GGTAAATTAA CATGTTCAAA GTCACGTGGC 120 TATTAAGTGG TAGAGCTGGA ACTTGAATAG GGTTTTTTTG ACTTTACATC TGGCACCTAA 180 GCTCCTCTGC CACATTCTTG AACTCAGTTC TCCAGCATAT CTCAGTGTAT CCAGAAGCAA 240 TTTTTCTCCC TTTTTCCTTT CCCCCCTCCT CCCCCACCCC ACAGGTCTCC ACCTCCCAAG 300 TCCACAAATG CCAAACTCAC AAGTCATCTG TTTTGCCAAA ATTCTGTTCC GATTTGATAA 360 ACCCTAGCTG GGCCAGCTCA CTCAGCATGA TTCAGCCGGA GAGAATAGCA AGGCTGCATG 420 CCCGGCATGC CGACCAGCTG AGCTCAGGCA GGATGGGAGG CGCTCAGGAA CCTCAGCCTG 480 ACAGATGGCT CCACTCGGCT GTCTCCACGG GCCTGATGCC AGGGGCAGCA CTCGTTCTCA 540 GCAGGAGGGA GGTCGTACGA GTTTCACATG CATGGATGTG TGTGTGTGTG TGTGTGTGTG 600 TGTTTCACAT GGACCATGCA GGAGTGAAGC TGTGTATTAT CCAGAGTGCC CATGTGTATG 660 TGGCCGGTTT GCACATGTTT GTCTGTATGC GTGTGGATGA ATGCATGTGT GCATGTCTAG 720 CTGTGTGTTT GTGTGTGTAT TTGTGTGCAT GCAGAAGTGT ATGTGTGTGT GTTTGAGTTT 780 CAAATTTGCA TTCATGTAGG ATGTGTGCTC ATGAGCATGA AAGAGAAAGC TGGGGGTGGG 840 AAGTAGGGGG AGAACGGTCG TGGGCTTTGA GAGTTGAGAA TGTTGAATGT TCCCACCTGC 900 AGTGGAGAGT TGCTGTATGC CCCTCCCTCC AGCTCTCTCT CCTCTTCACA GGACTGACTG 960 ACATCAGCAG CAGCAAAAGG TCATATCAAG CCCAATGTGA AGTTTAGGCT 1010
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