Tag | Content |
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EnhancerAtlas ID | HS116-06764 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr11:72898780-72899950 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXH1 | MA0479.1 | chr11:72899099-72899110 | TCCAATCCACA | + | 6.62 |
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| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_09800 | chr11:72895515-72903043 | CD14 | SE_10903 | chr11:72899050-72901663 | CD20 | SE_26760 | chr11:72896324-72899745 | Esophagus | SE_33919 | chr11:72898619-72899489 | HCC1954 | SE_40760 | chr11:72898722-72900096 | Left_Ventricle | SE_58465 | chr11:72849904-72901275 | Ly1 | SE_59666 | chr11:72848432-72901825 | Ly4 | SE_61154 | chr11:72849937-72901910 | HBL1 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH11I073187 | chr11 | 72899021 | 72901606 |
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Enhancer Sequence | CAATGCTTCT GCCTCAGCCT CCCAAGTAGC TGGGACTATA GGCACATGAC GCCACATCCA 60 GCTAATTTTT TAAAAAGTTT TTTGTAGAGA TGGGGTGGGG TCTTGTTATG TTACCAGGAC 120 TGATCTCAAA GTCCTGGCCT CAAGTGATTC TCCCTCCTTG GCATCCCAAA GTGCTCGGAT 180 TATAGGCATG AGGTACCACA CTCAGCCAGG ATCTGCATTT TAAATAAGAT TCTCAGAGCA 240 CTAAGGCAGA GCAGAGGAAA GTGGGTGGAG CTGCATGCCT GGGCAGGATG AGGCTGACTT 300 TGGGCCTGTC CCAGGTGTCT CCAATCCACA CCTCTATCAA TCAGGCTAAC ACACCTCCTG 360 GCTCCTCCTC TGCTCTTGGG AGTTGATGCT AAGGTGTGAG GTTATCCAGT TCAGCCTTGG 420 AAGGACAGGC TGGCCCCCTC AATCCTGTTC TAGGAGAACA AAAATAGTGA AGTCTCTCCT 480 TGGTTCCTCT CAGGGCTCTG AAGGGCTTGG GGCTGGGAGC CACATAGGAT CCAAGAAACT 540 AGCAGGGGGT GCCTCCTGCC CATCGATCCC CCTTCTGAAC CATGTTCATC CTAGCTTGTG 600 AATCTCCCCT CCCAGCCTCC GGGTAGGTCA CTGCCAAAAC TCTGGCTGAC CTCTTCCATC 660 TTGAGTGGGG TGTGGGCTCA GTCCCTTGGG GCCATGGGAG CCTGAAGCCT GGGCCAGATC 720 CCCCCTCCCT ATCCCTGTTG GGGCTAATTT TAGGGCTGCT TTGACAGCTG CCTCAGCTCA 780 GCCTGGGTCA GTTCCCAGCC ACTCACTGTT GGGGTCAGTT AGGGTCACCT AGGAGTGGGC 840 CAGGCCAGCC CCACCTTTGG CTGCAAAAGA TGAAACTAGA ATCTTTGTCC CCTGTCCGCC 900 CTCCCCACTG CCTGGAGAGT CCCACTGAGC TGACCTCCAC GTCCCATGCC CTGTATGTGA 960 AACCGCAGAG GAGCCCAGGA TTTAGAACAG CCCATGGAGA TCAAGACTGA GTATTGGTGC 1020 CTCCATGCCT GGAGGATGCA GACAGGTGAG GCCCCTTCTC AGCGGCCCTC TCTGATGCCA 1080 ACCCAACACA TATTTCTGAA CTCAGTTACT GTGCAAGGCT GTCAGAGATT AGGAGCAGAT 1140 GACACCTGGG ATACTTTCTG TTTTTTGAGA 1170
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