Tag | Content |
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EnhancerAtlas ID | HS056-07523 |
Organism | Homo sapiens |
Tissue/cell | GC_B_cell |
Coordinate | chr19:12095600-12096260 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myog | MA0500.1 | chr19:12096030-12096041 | AACAGCTGCAG | + | 6.02 | STAT3 | MA0144.2 | chr19:12096153-12096164 | TTTCTGGGAAG | + | 6.02 | Tcf12 | MA0521.1 | chr19:12095701-12095712 | AACAGCTGCTG | + | 6.32 | Tcf12 | MA0521.1 | chr19:12096030-12096041 | AACAGCTGCAG | + | 6.62 |
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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 |
GH19I011985 | chr19 | 12095861 | 12096010 |
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Enhancer Sequence | GCATCAGATC CATGCCCGAG CTCTGTGGGC GCTGCTGCCT CTCTCCACCT CAGGCACCAC 60 ATCCCAGGAG CCCCAATCCC ACTGCCTGGC TTGTGCTTTA GAACAGCTGC TGCTGCAGGG 120 CCCTCAGCTG CCACTACCAA GTTGCGATTT AGAAGTCTTT TAATGCATTT AAATATCTTA 180 GAATTTGTCT TCCCCACTTT ATACACACAA TCATGAGGAG AGCAGGGACT CTATTGGTGT 240 CTTATTCACA CAGTGGGATT GAGGGTGTTT GTCTCATGAA ACTGATCAAT GAAGTGAGAA 300 ACAGCTGAAT AACCTACAGG GGGCAGCAGA GCCTGAGGCC AGTGTGGGCC TGCAAAGGAA 360 GGGAAAGGGA GTTCCTTGGG GGCTTCCGGG GCTCCCCGCC TTCCCCTGCA GGTGGCCTCC 420 AGCTGCCCAG AACAGCTGCA GAGAGTGTGG ATTCTGAGAA GCTGCAGGGC CCTGGAAAGC 480 AGGAGACCCA CGTGCAGGTG CGCTTAGGGG GTTCCATCCT TTCTGAGGTT GCCCTTCTGG 540 AGCCTGGGGC CATTTTCTGG GAAGTGTTTT GGTTTTGACA TGTATAGGGT CGCTGGGGTC 600 AGAATGTAAT TGTTACATAT GAAGAAAATC TGTGAAGGTC AGCCTCAGTG AGACTTGTTG 660
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