Tag | Content |
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EnhancerAtlas ID | HS116-13755 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr16:70623820-70625370 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXH1 | MA0479.1 | chr16:70624269-70624280 | TGTGGATTGGG | - | 6.14 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_27048 | chr16:70623158-70626711 | Esophagus | SE_29256 | chr16:70622975-70627455 | Fetal_Intestine_Large | SE_54230 | chr16:70621344-70626697 | Spleen |
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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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Enhancer Sequence | CGGCCTTACC ATGATTTTTA AAAACAAACG AAAAAATAGT AGATCCTTTA CAGGGTTCGT 60 GAGGACAGGA TGAGGCAACG CATGTGAACT GTGTTATTAG CCTCAGGTCT GTGGGAATAC 120 AAGGCTTTCT GCCTTCGGGG AGGTGTTGCT GGAGAGATGG ACAGACCCAC CCAGGGGAGG 180 GGCGTCTGTG TCCCTGTGGA AGTCATTACT CCATTCAGCA GAAGCTGCTC ACGGCGGGAG 240 AGGGCTGGGG TTCAGGGAAT CCTTCCTGGA GCCGTGATGG GGCCCTGCTT GGGGGATTCC 300 TAGCATGTGT GGGATGGGCA GATTCCAGAC ATTGGAAAGT CCCTGGCAGA AAAATCACTC 360 CCACTAAGGG GCAGTTGTAG GGAAGAGATT TGGGCTCACG CTAGAGAACT CATGATCAGA 420 GATGTCTGCA TGAGGAACAG AGGCTGCTTT GTGGATTGGG GAGCTCCCCA TTAGCGGAGG 480 CAGGTAAGGA GGTGCCTGTG CGAGGTGGGG GTGGAGCCAA GGCTGTGTAC CTCCGACGCT 540 GTGCACCTCT CTGATGGGAC CCAGTCCAGA CAAAAATTGT ATATAACAAA CCCTTGTAAA 600 GGTGGTGCTC GGGTCAGAGG GAGGGGGCAG CCGGGTGGGA AGGCTTGTCC CAGGTCTAGC 660 CCAATAGTGC GGAAGTAGCT GGTGCTGTTT TCACTGGGCC AGGTGCTGTG TTAAGCTGAA 720 CAGGCTTGAT CTCAAATCCT CACCATAGCC CTGTGCGGTA GGGGCTGTCA ACACCTGGGA 780 ACCAAGGCTC AGAGGTTAAG TCACCTGCCC AAGGTTAGCC AGCAGCTGGC GTTGCTGGGA 840 TTCGAACCCA GGCAGTCCGG CTTGAGCCCT CCATCCTGGG TGGAAGTCTC CCAAACCCGT 900 CCCCCCGCAA GCTGGCCTCT CCCTGCCCCC GCCCCTGGCA GTCAGTTCCT GGGGTCAGGG 960 GTGCCCTGCC ACCCCCACAG TACAGATGTA GCTGCTGTGC CCTCCCCGTC GTCAGTGCGC 1020 TGCCCCTCCC TCTGGCTGCC TTCACACTGT CAGCGCTGGC TGCTCTGTGC AGTCAGACCC 1080 GGCCCCGGCC CCAGCCTGCT CGGGTCTCCG GGGTCTCAGG ACAGCACTGT GGGGACCATG 1140 CCAAGCGAGA CTGGGAGAGC CAGGCTCCGT GTCACTCAGT GCCTTCCTTC TCCTGCCATT 1200 CAACGAGACA CTCCTAATAA CTCTCTTGCA GGCCTCTAAG TCTGTCCCAT AGCTGTTGAG 1260 CTGATTTTGC CTTTTGTGCA ACTGTGTTTT CCAACTCAGC TCTCTGGGTG CCAAGACCTT 1320 GTCCACATGA TTCAATCTGT CCAACTCCAA CCTGGCCCCT GATAGGCCAT AAATACCATT 1380 CCTGATGGCA GTGATCCAGT GCCCTCCTTT GTCCCCAGAG CTGAGGCAGG ATGACCACCA 1440 CGCTTATAGC TAGGACAGAG GGTGACTCTG GCAGGGACAG CAGTTTATCC AGAATGACCC 1500 AGTTAGCCGG GCGTGGTGGC ACGTACCTGT AGTCCCAGCT ACTCAGGAGG 1550
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