Tag | Content |
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EnhancerAtlas ID | HS187-04644 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr11:72125120-72126180 |
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 | GAAGCACAGA TTCCCAGAGT GACCTTCTGG GATCCTCTAT AGCAAACATC TTTGCTTCCC 60 CAGGCAGTGT GTGCCAAGGC TGAGACTGAA TAAAACACGG AAGTCCAACA ATACAAGGCC 120 ATAAACAGGA GGGAGTGGCC CAAAGCACCT TCATCTGGGT ACCCCTGCCC AGAGCTATTA 180 ATATATGCAT TTCCCAGAGA GTCAGCAGCT GTGGTGGTGA GAAGGAAAGG CCTGTGCAGG 240 ACCTGAGGTG TGGGAAAGGG TCATAGGCGC CACCTACTGG CCCCACAGCA GGCCTCCTGG 300 CTGGCTGCCA GGAAACCTGT CACACTACAG CAGTGAGACA CAAAAGTGGT TCAAATTTCT 360 CAAACAGTGA AACAGTGTTG GTACTTGAGC CACCTTCTGT GAAGTTCAGG AATCTCACAA 420 AATTTCCAGT AAAGAAGAGA CAATGAAAAG CCAACCATAA AACCTGGCCT CCTCGGGCAA 480 AGGTGTGGCC TTCACTCACT CAACAAAACT GAAGTAACAT CTCCAAGCTA GCCTCTGTGT 540 TGGGCATTGA CAGACACCGA AGTCAATCAG ACATGAATCT TGCCTACAAG GAGCTCTTAT 600 TCTGAGCTGG AGGAGGGAAA ATGAAACAAG CGCACAAATA AGTGCACTAA GTATCACAGG 660 TGCTCAGAGA TGTTTACACA GGCTCAGGGA GCACAACTCA CCGCCTTGCA AAGCTCTTGA 720 ATGATGGAGT TCAAAAGAGC TCACATTTCT TGAGCTGCCT ACTACGCAAC AGATACTTGA 780 CATTTATGAT CTCATTTGAT CCTCTGAAAG AAGCCCAAGT CTTACAGAGG GTAAATGACT 840 GATTAAGATT ACAAGGCCAG GCTGGGAACG GTGGTTCACG CCTGTAATCC CAGTACTTTG 900 AGAGGCCGAG GTGGGTGGAT CACAAGGTCA GAGGTTGAAG ACCAGCCTGA CCAACATGGT 960 GAAACCCTAT CTCTACTAAA AATACAAAAA TTAGCCAGGC ATGGTGGCAG GCACCTGTAA 1020 TCCCAGCTAC TCAGGAGGCT GAGGCAGGAG AATCACTTGA 1060
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