Tag | Content |
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EnhancerAtlas ID | HS116-12878 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr15:99948370-99949700 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr15:99949625-99949640 | AAGGTCAGGAGTTCA | + | 6.04 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_40746 | chr15:99947898-99950344 | Left_Ventricle |
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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 |
GH15I099407 | chr15 | 99947993 | 99949805 |
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Enhancer Sequence | GAAGAGATTC TCCTCGGATT TTTTTAAGGA ATAATGAAAT GTGCCTGGTA TATGACAAGG 60 CCTCAAAAGG AAAGCTTCTC CCCATTCCCT GCCATCCCCC AAACTCTGCC CACTCCCTCC 120 TGCCCACTCC CTCCCTCTCT TGGGCGTGGC TCAGTATTTA TCTTCATTCC CTGGAGCTGA 180 GTTGGTTGGA GGGAGAGGGG TGCTGTAGGA AAGCCCTCCT CCTGTCCCCA GAGAGATAGC 240 ATTCCCGAGG GGCTGATTCC AGCCTCCGCT CGCATCACAC TCCTGCCAAG CCTGCGGCCT 300 CCTTTTTTCT CCTTATGGCT CAGAGCCCAG TTTTGGAGAC ATTTGGCTCT GATGCACTTC 360 TAAGTGCTGA GACAAGTTAC TTGGATGCCT TTAAACCCAA AACAAGGTCA GACATCAAAC 420 CACATCTCGC TGTGCAGCCA GGCTTCCACT CCCAGCTGCC CCAGGGAGGT GGTGGAAAGA 480 ATAAACAGTA TTAATGGTGG AGCTAATATT GTGCCCACCC AGGCTCCAGG CCCTTCACCA 540 GCTGCAGCCA CTCTTGCTGA TGGTAGTCTG GGGTCTCTCT GTTTATTTGC TATATGTTTG 600 CACTCGTAAA TGTTGCGCAT CTTATATAGT ATGGTTTTGT GGGCATTGCA CGGATAATAT 660 TGTTCTTCAA CTGTGCTTTC ACTAACTTGG CATTGCTGAG ATGAGGCCCT GTGGATAAGT 720 TTTGTGCATG GTTCCCCTGA GCTCCTGGCT GCCGCCTGTC CTCCCCAGAA ATGGCCAGCA 780 TTTGCTGACT CTGAGGCAGT GTCTGGCCAA GGAGTGCCTT TCCTTCCAGA GCACAACACG 840 ATCACTTTAA TGATAATGTC ACTTAAAGAT ATAAAAAAAC AAGGCACATT TGCCTGATTT 900 GAAGCTGAGA GCATATTCCG TATGCTGGTT TAGGGCTGCA GAAAAGTTTT TGGTGCCAGT 960 GACACATACA CAGCACTGTT TCCTGATCTG GGTCATGGTG ACGGCCGTGG CACCCTGAAA 1020 AGCACCTAGC ACCTAATACT GGCAAGGGGT AGAGGGAGCT CCAGAGCCAG GGCTGGGCTG 1080 GAGATTGCTG CTCTTCCTGC TCCTCCCGTG TCCCCAGCTG CCAGAGGGAA GCTGCTGCCT 1140 TCCTGTTTAA ACGCATCTTA AATCTGTGCT CATCAAAAGC ATCACCCAGG GCCGGGCACG 1200 GTGGCTGACG CCTCTAATCC CAGCACTTTG AGGGGCCGAG GCTGGCGAAT CACCCAAGGT 1260 CAGGAGTTCA AGACCAGCTT GGCCAACATG GTGAAACCCC GTCTTTACTA AAAATACAAA 1320 AAAATTAGCC 1330
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