Tag | Content |
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EnhancerAtlas ID | HS063-01632 |
Organism | Homo sapiens |
Tissue/cell | GM18505 |
Coordinate | chr13:111123120-111124530 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr13:111124412-111124430 | GCTGCCTTCCCTCCATCC | - | 6.38 | RUNX1 | MA0002.2 | chr13:111123372-111123383 | CTCTGTGGTTT | + | 6.14 |
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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 |
GH13I110470 | chr13 | 111123251 | 111125025 |
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Enhancer Sequence | AGATAGCTGA TTTAAGCCTC AATGCAGAAG TGTCTGTCCG TCCCTGATAG ATGGTATCTT 60 TCGGAATTTT GTGTTGCAGC CCGTAGGGAT TGTTCCAAAC CCTGACCCTG TTTCCTTTCA 120 TATGATGCGT TTCTCCATGT TTTGCAAAAT TGGGAAGCAG GCTTCCTGTG TCTGTATCAA 180 GGCCCTGGTA AAAACAACTC TGCATTCGAA TGAAGCAAAG GAAGTCTCCA TGCCTCTGCC 240 CCAGGGGTTG GTCTCTGTGG TTTTGTTGCC CTGCTGGAAG TGTCTAAATA TTTAGAAGTG 300 TAACATTGCC ACTCTCATGA TTTCATATAT ACTAAGTTTA AGCATTCATG ATTTTGAGAG 360 AAGGATAATA ATTCCTGAAC AGCTTCTTGC TGTGAGTATG AAAGTTCTCT GGTAATTGTG 420 ATTGGAGTGC CCAGCCATGT GTGCGTGAAC GCCACACGGG GCTCCCCTGT AGGGGGGAAT 480 GGATGGGATG CACCCATTAT CAGGTGATTT GGACAGTTGC CCACGTGAGT TGGGAGCCTG 540 TTCCACCATC AAATGTGAGC CCTTACGTCA TGAACAGGGA GGCTGGGGCA GGCTGGGGGT 600 GGGTGGTGAT TGAGGAACTG ATCAGTTTCT GAAACGCATG TCACTTTTTA TGGTGCTGAA 660 ATATACTGCC CTTCTGTCGC CACATGCAGA AGAGGATAAA ATGCCCAATT CAAGGATTGC 720 AAAAATCAGA GAGTCTATTC CAGATCTAAG ACCCACACAT GCAAACCCAA GTGCATGGCT 780 CCCTGGGTAC AGTTTGTAAC ATTGCCAGTG AAAGTCATGT CTCTTCATTG TGAGTAAATC 840 ACACCGTTAA AACTCTGAGT ACGGTCTAGC TGATTAACGT CAGGTTAATC CAGATCCTTT 900 ATTCTGTATT CCAGTTACTC CCAGCTCCCA GGCAGTGATG GCTTTACCGG CCCAGGAGGT 960 CCCCGGGCCC TGCTCATTGG ATCTTTTTGG TGGGATACAC CCCACAGAAC ACAGAAAACA 1020 TTCCCTTTTC CGTATCCATA CATAGGAGTG CCGAGCCTGC CGTGTACTTG ATCTTGTCCC 1080 ACAGAATCAC CTGCCAGTCT CATCGTTGCA GGCTTCTCTC CTGCATGCAC AGCGGGGGTG 1140 GTGGTGACCT CAGAAGCCTT TCCTTCTGAG CACTGCGTGA CTGTCAGCTG TGGGAGTTCA 1200 TTCTGAGGCC ATGTCAGGGC TGACTGCACC GAAAAAGGAA GTGACCTGAT GAGATCATTT 1260 TATCCAGTGG CACCCACAAA AGACACAGGA CAGCTGCCTT CCCTCCATCC GCAGATGGGA 1320 CTTGATGATT TTCTTTTTTC TTTTTATTTT TTTCTCTTTT GAGATGGAAT CTCACTCTGT 1380 CGCCCAGGCT GGAGTGCAGT GGTGCGATCT 1410
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