Tag | Content |
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EnhancerAtlas ID | HS101-18892 | Organism | Homo sapiens | Tissue/cell | HT29 | Coordinate | chr17:48004200-48004920 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr17:48004566-48004584 | CCTTCCTTCCCGCCATCC | - | 6.76 | Nr2f6(var.2) | MA0728.1 | chr17:48004236-48004251 | TGACTTCTTGACCCT | - | 6.24 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTGTCAATGT GTCCAGAGGC AGGGAGATGC CAGAGATGAC TTCTTGACCC TCCCAGATGG 60 CCCTTTGGGG CCTCCTGGGC CCATCCAAAG CTCTGCCCAC CAGGCGTGGG TGGCTGGACT 120 GTGGATGGTT GGCTCAAGCC TGCATCATTT GGACGGCGCC AACCGGGCCA AAGGTGCCCC 180 ACACATTGCC TGTCCCGGGA TGGTGTCCAG GCCTTGGTCC CCAGGGTCCT CCCACCCCTG 240 CTGGACAGCA GCCTCTCCCA GTGACTCAGC CCTGACGTCG TGGGGCGAGC GGAAAGGCCA 300 AGGGCGTGGG AGGTGGTGGC TCCCTCCCTC CTGTCCTCAC CTCTCTGGGT TCAGTCCCCA 360 TAACCTCCTT CCTTCCCGCC ATCCCCGTTC TTTCATGAGC CTCTGTGCAG GAGCTATTGC 420 CCCGGCCCAT GGAGACATGC CCTATGTGTG CCCAGGTGTG TGCCAGGCCA CCGTGGGTCA 480 TGGGATACAA GAACCACAGT GTGAGAGAGC TCCTGGCTCT GGATCCCACT CCCTCGCCCC 540 TCACCCCAGC AGTCCCACCC TAATAGAGGG TTGGGGGGCA CCAGCTCCTT TCTTAGGTGG 600 CCTGGGGCAC TCTCTGTTCA CACTTGGGGA TCTCTGTGCC CCAGGCCCTG GATCCACTTG 660 TCTGCCCCCT GCCCTCCAGG GCCTCCCTTA GGTGTGTGAT CTCAGCTTTT TTTATCTCCC 720
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