Tag | Content |
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EnhancerAtlas ID | HS098-28385 | Organism | Homo sapiens | Tissue/cell | HSMM | Coordinate | chr19:50475830-50477030 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr19:50476312-50476330 | AGGAGGAAGGCAGCAAGG | + | 6.15 | Zfx | MA0146.2 | chr19:50476174-50476188 | GGGGGCTAGGCCTG | + | 6.41 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 50476470 | 50476531 | chr19 | 50476843 | 50476923 |
| Enhancer Sequence | TGAATGGGCC TTATCCCACT TTTCCAGGCA AATCAGGGCC CATGACGGGG GTGGTTCTGG 60 TGGCTGTTGG GGAGGTGGCT ATGAAGATCC TGCTTCTCTG CCTCTGCCTC ATCCTCCTCA 120 GGTGAGCCCT GCCCCAGGGA CCAAGGGGAG GGGCGGAGAG GGCAAAGGAT ACACCGCTGA 180 ATCCCAGAAT CTCAATCCTG GGGGTACTTG GACAGTTAAA GAGGCCTGTG GCCAGGCAGA 240 GGCTGAGTTG ATCGTGATGA TTCCACACGG GCCAGTGTTG TCAGTCCCCA ACTCTGGACC 300 AATGTCCAGG CTGGGGAGGT TCCTGCTTGT ATCAGGGAGG TCCTGGGGGC TAGGCCTGCT 360 CTCTCTGCCT CAGTCCCCTC CAACCCCTTA GCAGGGCACA GGGAGGTGAG TCTGCTGCCC 420 TCTTCACCCC CATCCAGCCA CACTCACAGG CCCTGGTCTC TTCACCCAGA GTGAGGTCTT 480 GCAGGAGGAA GGCAGCAAGG GCAGCATTGG GCATGGAGGC TGCAGACGCT GTCACGGACT 540 AATCTCCAGG TGAGTGTCGT GGGCCTCTTA CCCTCCAACA TCCCGCTGGA CACCTCCCCC 600 TCGATGGCCC CAAGGACTGC TCCACTCAAC TTGGCCATAA CTGACTCATC ACCTCCCTTT 660 CCAAGCCCAC TTCTCTTGTT GAGAGCCCCA TCCCTCTGAT GACATGGTAG CCCCATCTCT 720 AACGTCAGAA CCCGGGTGTG GGTGTCCACC TTGACCTCCC TCCCTCCTCC AGATCCCAAA 780 AATCACTAGC ACTTGTCCCT CCTCCTAAGT ACAGGTCACC TTGGAGCCCT TTTCTCCATC 840 CTGGCCCCGG TCATGCCTGG GCCTCACCTC TTCCCTGGTC GCTGAACCCA CCTCACCTCT 900 TGCCTCCATC TCTCCCAACA GACTCCAGAC TGCTTCCAGA TGCCTCCTCA TCCAGTTCCT 960 CCACAGTCTG AGCGGCCGTG TTTCCTCTGC AGGCTTTGCA TGGTCTGTCC CCTGCTGGAC 1020 TCTCCTGATC CCTCCTTTCC CTGTCACCCA ACATCTCCCC AAACCCTCCG GGCCAAGGAC 1080 TCTGCGGCTC TTGACACTTT GCACGTGTAG TTTCTTCTCC TGAAACACCC TTCCCTCCTG 1140 CCAAACCACG TCTGGACCCT CCTTCAGGTT CACTTTTTTT TTTTTTTTTT GAGACACAGT 1200
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