Tag | Content |
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EnhancerAtlas ID | HS010-03675 | Organism | Homo sapiens | Tissue/cell | B_cell_blood | Coordinate | chr5:149061930-149062630 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr5:149062285-149062303 | GGAAGGAAGGAAGGAAGG | + | 10.83 | EWSR1-FLI1 | MA0149.1 | chr5:149062293-149062311 | GGAAGGAAGGAACAAATG | + | 6.79 | EWSR1-FLI1 | MA0149.1 | chr5:149062289-149062307 | GGAAGGAAGGAAGGAACA | + | 8.32 | EWSR1-FLI1 | MA0149.1 | chr5:149062281-149062299 | TGAAGGAAGGAAGGAAGG | + | 9.09 | ZNF263 | MA0528.1 | chr5:149062282-149062303 | GAAGGAAGGAAGGAAGGAAGG | + | 6.94 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CCCACTAGCA ATGGCTTGGT CAGAGGTCGA GCCACCCTGA CCTCTCGGGC CCTTGCATAC 60 GCAGTTCCAT CTGTCTCAAA TGCCCTTCCC TCTGCGCTGA ACTTGGCCAA CTCCTGCCCA 120 GATTAATAGC TCTTTCCTCA GAGAAGCCTG ACCTGGCCAG ATTCAGTCTC ACCACGCCAT 180 GTAACTCTGT CTTACAGGCT CTAGCACAGT TGTTATGGAA ATGTGTGTTA GAATTTATGG 240 TATCTGTCTC TGAAAGGAAT GTAAGCAGGA ACCGTGTCTA TCTTGTTCAC CGAGATATTC 300 CTGCAACTTA GCCCAGTGCC TGGCACATAG TAAGTGTTCA GTAAGTACTT TTGAAGGAAG 360 GAAGGAAGGA AGGAACAAAT GAATGAATGA TTTGTCAAAC GTTGACTGGA TGATTGAACC 420 AGTGATCTCA AATGCATTTG GCTGATGGGA TGTAGCAGCC GTTGTGCAGA GCAGGAGGGA 480 GGCTGAGGGG AAGATGCTAC CGTGAGAGAC AGTGCCTCCC TGGGGGCGGT GACAGAGAGA 540 GAGAGGAAGG AACTGCATGG CCTGTGATGA ACTAGATTAC CCCAAGACTC CATCCAACCT 600 TGAAATGCTG TTACTTGATG TGAGGATGGG CTGGCGTCCC AGATGTCAAC CCTTTAAGGT 660 CATGGTCCCC CAGGCCCTCC TCGTTTACCT GAAGAATCCA 700
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