Tag | Content |
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EnhancerAtlas ID | HS041-20469 |
Organism | Homo sapiens |
Tissue/cell | EWS502 |
Coordinate | chr8:123733510-123734870 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr8:123734325-123734343 | GAGAGGAGGGAAGGCAGG | + | 6.39 | EWSR1-FLI1 | MA0149.1 | chr8:123734329-123734347 | GGAGGGAAGGCAGGACAG | + | 6.39 | IRF1 | MA0050.2 | chr8:123734808-123734829 | AAAGAAAAAAAGAAAGAAAGA | - | 6.34 |
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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 |
GH08I122721 | chr8 | 123733314 | 123734770 |
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Enhancer Sequence | AGGGCCTCGA GGCCTGCTTC TGAAGTCTTT AAACCACAGC CCTCTGAACT TGGGATCTGA 60 CAGGGCCTTG CGGCTCTCAG AGCCCTAGTG GGAAACAACA TAACCCTACC AGGTAACAAC 120 TGTGGCCACC ATTGTGGACA AGCCCCGAGA GACCACTCAT GTCTATTTAA CTTCCCTGTC 180 ACAGAGCGTC ATACACCGCC AGGCCCAGAC AGATACTTAA TATGTCCCTG TGATGAAAAT 240 CTATGTAGCT GGAAAAGTAT TCATTTTCCC TGCACCTACC TAATATTTGA TGCCGACACT 300 GAGCCGGCTG GAGGCAAGCA ACAAGAATGA TTTAATAAAA GTGCAATTGA AACGCAAGGC 360 AAAGGAGAGA AAGTGAGAAA GGCAGGCCAG GCAGCAGCTA AATGTTTGAA ACCAAGGCTT 420 TTATGTCTTT GAAACAGAAT CCAGGAAAAT TGCTGCACCC TCTGTAGATG GCTGGAGGGC 480 TTTTTCCTCT GGATGGTTGC TTCGTTTGGG AGCCTCCAAT CTCTTGTCTC ACAGGTTGGG 540 AGTGTAGCCC TGAAGTCTCT GTGCAGCAGG GTGTGTGTGA ATCAGTCTTG GGAGCTGGCA 600 CGGCCCTGGG CCTCGCGTGG AGTCCAGGCC AGGCTCTGAC ACACTGAGGA GAGTTGAAAC 660 GAGAGTGGGT GTTTGCTGAC AAGCAGCTTC ATGGGAACGC TCTCCTTGGC ATTTCTCAGT 720 GCTGAATCAG GGAGAAAAGT TGGGCAGATT GCCTGTGAGG CTCAACACAC ACACACACAC 780 ACACACACAC ACACACAGAG AGAGAGAGAG AAAGAGAGAG GAGGGAAGGC AGGACAGAGG 840 GAGGAAGAAC CAAGTCAGAG TTAGGAGAGC AAACACCACA CAATGCAGTA ATGGCAGTAG 900 CAAAATTATC ACTTCCTGAG GGTCTCCTGG GTGCTTTCAG TGAACTCTCC CTGGGTGTCC 960 TGGGGAAAGC TTTATGCATA AAGAAACCCC TGGGGGAACT TTATATACAT ATATATGTGT 1020 ATATAAAGTT TATATGGCAC ATGAAAAAAC TCACACCTCT AATCCCAGCA CTGTGGGAGG 1080 CCGAGGCAGG TGGATCACCT GAGGTAAGGA GTTCAAGACC AGCCTGGCCA ACATAGCGAA 1140 ACCCTGTCTC TACTAAAAAT ACAAAAATTA TCTGGGCGTG GTGGTGGGAA GCTGAGGCAG 1200 GAGAATCGCT TGAACCTGGA AGGCAGAGGT TGCAGTGAGC CGAGATCGCA TCACCGTACT 1260 CCAACCTGGG TGACAGAGTG AGACTCCGTC TCAAAAAAAA AGAAAAAAAG AAAGAAAGAT 1320 TCAGAGCTGC TCAGCTACCT GGTGGCTGAA ACAGAATTCA 1360
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