Tag | Content |
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EnhancerAtlas ID | HS193-28103 |
Organism | Homo sapiens |
Tissue/cell | U87 |
Coordinate | chr5:95965100-95966570 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr5:95966545-95966563 | GAAAGAAAGAAAGGAAGG | + | 7.02 | EWSR1-FLI1 | MA0149.1 | chr5:95966549-95966567 | GAAAGAAAGGAAGGAAGG | + | 8.57 |
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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 |
GH05I096626 | chr5 | 95961723 | 95966734 |
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Enhancer Sequence | CAGTATTCTT TCCAGCGCTC CCCTCTGGGT GGGCCAAGAC TTTGCCAAGC CTCCATTTTG 60 GTTCAGTTTC TCCCACAGCT GAGTCCTTCT TCCATTCGCA GGTATTAATT CCTTATAAAT 120 ATCTTGTACC ACAAACTCTG TCTCAGCATC TTCTTGCTAA AAAGTATGGG TTGGCACTTT 180 GCCTCAGTTT CTTTCAGACA GTGAACATAG TGCTAAACAG GAGGGTCTTA GGCCAACCAA 240 CTTGAAATCA AACTGTAACT TATATCTCAA TCTTTCCTTC CAATCTCATT CTTTAACCCT 300 CCCTATCAGC ATCTGATTCA AGCAACATGG GTTTGTTCAC CTCCCACCTT TAAAACCCAC 360 TGCTCTGCTG TCTGGGAGAA ATGTTTTCTT CATCACTCTC TGCCTAAACT TGATTAATCA 420 GGCTAAGCAA TGTACCACAG CACTTATTTA GTGTTGATTT TGGCAGAGAT GAATTTCTTC 480 TTCTATGAAG TACTATGAAT TTGCAAACAC AGATTTAAAC CACAGCCAAG CCCTAAACCA 540 GCTAAGCCTG CAGTACGGTG GACTAGACTC AACAGGATTA CAGAACAAGG CAATTCCAGG 600 CCACTTCTGG GCCTGCCTGT AACCTGAGAA GGCTTGAGAT ATCTGTCACA GCTTCCTGTC 660 TTCTCAATTA GTCATTCATT CAAATAATAT TTATGGAGCA CTGTCCTAAG AACTGGGGAT 720 GTATCATTGA ATAAAACAAT CATGTTCTCT GTCTTCCGAG CTTACAGTCT ATGGTTAGAG 780 ACAAAAATCC AGCAAAGAAG CAATTAACCA TAATTAGCCA TGCAGGATAC TAACAGAATG 840 CAGTGACGGA AAAATGAAGG TGATAAGTGG GAATCTATTA ATACTTAGCT ATCAGGGAAG 900 TCTTCTCTAG AAAAAGACTA AGTTGGGCCT GAAAAATAAG AAAACACAAG CCATGGGAGA 960 GTCAGGAAAG AGCATTCGAG GCAGAGAGGC TACATCAAAT CATTCTTTGT TTACTGAACA 1020 AGTAAGTTAC TTCTGAGCTA AGCATTAAAA TACAGGAGGG AAGAAAACTA ACTTCTAAAC 1080 AAGTGAATAA AGTATCATAC TCCCTTGAGG CCAGGTGCGG TGGCTCATAC CTGTAATCCC 1140 AGCACTTTGG GAGGCTGAGG AGGGTGGATC ACCTGAGGTC AGGAGTTCGA GACCAGCCAG 1200 ACCAATATGG TGAAACCTCG TCTCTACTAA AAATACAAAA TTAGCCAGTT GTTGTGGTGC 1260 ATGCCTGTAA TCCCAGCTAC TTGGGAGGCT GAGGTGGGAG GATTGCTTGA ACCTGGGAGG 1320 CGGAGGTTGC AGTGAGCCAA GATTGTGCCA CTGCACTCCA GCCTGGGGGA CAGAGCAAGA 1380 CTCCATCTCA AAATAAAATA AAATAATGAA GTATCATACT CGAAAGAAAG AGAGAGAGAA 1440 AGAAGGAAAG AAAGAAAGGA AGGAAGGAAG 1470
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