Tag | Content |
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EnhancerAtlas ID | HS184-05947 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr11:72125010-72125930 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr11:72125384-72125403 | AGGCGCCACCTACTGGCCC | - | 6.57 | Foxa2 | MA0047.2 | chr11:72125790-72125802 | TGTTTACACAGG | + | 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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| Number: 1 | ID | Chromosome | Start | End |
GH11I072413 | chr11 | 72124821 | 72125984 |
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Enhancer Sequence | TAAAATACAA GCAAGGACCC TAGAGGAAGG TGCCATGAGA GTACAGGTCA GAGCAAGAGA 60 GCCACAGGGA TGACTTCCTA GAGGCAGAGT GTGCCAGAAA GGATGGGCCA GAAGCACAGA 120 TTCCCAGAGT GACCTTCTGG GATCCTCTAT AGCAAACATC TTTGCTTCCC CAGGCAGTGT 180 GTGCCAAGGC TGAGACTGAA TAAAACACGG AAGTCCAACA ATACAAGGCC ATAAACAGGA 240 GGGAGTGGCC CAAAGCACCT TCATCTGGGT ACCCCTGCCC AGAGCTATTA ATATATGCAT 300 TTCCCAGAGA GTCAGCAGCT GTGGTGGTGA GAAGGAAAGG CCTGTGCAGG ACCTGAGGTG 360 TGGGAAAGGG TCATAGGCGC CACCTACTGG CCCCACAGCA GGCCTCCTGG CTGGCTGCCA 420 GGAAACCTGT CACACTACAG CAGTGAGACA CAAAAGTGGT TCAAATTTCT CAAACAGTGA 480 AACAGTGTTG GTACTTGAGC CACCTTCTGT GAAGTTCAGG AATCTCACAA AATTTCCAGT 540 AAAGAAGAGA CAATGAAAAG CCAACCATAA AACCTGGCCT CCTCGGGCAA AGGTGTGGCC 600 TTCACTCACT CAACAAAACT GAAGTAACAT CTCCAAGCTA GCCTCTGTGT TGGGCATTGA 660 CAGACACCGA AGTCAATCAG ACATGAATCT TGCCTACAAG GAGCTCTTAT TCTGAGCTGG 720 AGGAGGGAAA ATGAAACAAG CGCACAAATA AGTGCACTAA GTATCACAGG TGCTCAGAGA 780 TGTTTACACA GGCTCAGGGA GCACAACTCA CCGCCTTGCA AAGCTCTTGA ATGATGGAGT 840 TCAAAAGAGC TCACATTTCT TGAGCTGCCT ACTACGCAAC AGATACTTGA CATTTATGAT 900 CTCATTTGAT CCTCTGAAAG 920
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