Tag | Content |
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EnhancerAtlas ID | HS138-00174 | Organism | Homo sapiens | Tissue/cell | MSC_BM | Coordinate | chr1:11376340-11377570 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr1:11377150-11377171 | CTTTACTTTTTTTTTTTTTTT | + | 6.01 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH01I011316 | chr1 | 11376903 | 11377179 |
| Enhancer Sequence | TTACAGATGA GGAAATTGAT CCCTTGCCTC TGCCTCCCCG AGTTTCAGTC CCACAGCTAG 60 TAAATGGTCC AGGCTGGCTG GAACCAGGTC CTGACTAGTG CTGTGGTGTC AGAGGCCAGT 120 GGGCAGTTCA GCTAGTGCCG CCAGGCTCTC CGAAGGCCAT GTCTCCAGAC AGGATGTCAG 180 GGCATGGGTC CCTGCTGCTC CCTTCCCCCT GGACAGGGGT CCTCTCAGGT GGCTCCCCTC 240 TGCTTTGCTC TGCAGCCCCA GCCTCAGGTG CTCCTACGCC AGCTCCTCCT GCCCACCCTT 300 TCTGTTCCCC AGGGCTGCCC TAAATGCTCA GACAGACTAA TTACAAGCAC GGGCAGAGAA 360 CTGGGCTGCT GATTTGGCAG GTGGGGCTTT AGGACTCCGT GATGCTCACC AGCGGCCGGC 420 AGGCTCCCTG ACACATCAGA GACTTTTCCA TTTCCTTTCC TCTCTCCTTC TCTTGCCCCT 480 GGAGGATGAG CCAGCCTGCC AGCAAGTGAG CGAGTGAGCC AGAGGTGGGC TGCTGAAGTC 540 TGTGCAGCAT GCTGGCTGTG GAATGAGAGG GCTCTGAGCA AGCCATGTCC CAGGAGAACT 600 TTTACTCAGG AATAATGTGC ATGAGGATTT ATTTCCTCAT TGCTGGGCTT CCAGCTGAAG 660 TACAGGCATG TCTCTGCTTG GCTCCGGCAG GGGAACTCGG CTCAAAGGTT TCAACAAAGC 720 AGCCAAAGAT TCCGATTCAA TGAACACTGA GCACATTCTG TATGGGAGGC TCCGTGCCGA 780 TAGCTCTGCC CACTCACCCC ATTTAACTTC CTTTACTTTT TTTTTTTTTT TTTTTTTGAT 840 ATTGGGCCTC CCTGTGTCAT CCAGGCTGGA GTGCAGTGGC ATGATCATGG CTCACTGCAG 900 CCTCAAACTC CTGGACTCAA GCAATCCTCC CGCCTCAGCC TCTCTCCTGA GTAGCTGGGA 960 CTACAGGCAC AAGTCCCCAT GCCTGGCGAA TTTTCAAGCT TTTTGTAGAG ATGGAGTCTC 1020 ACTATGTTGC CCAAGCCAAG TCTCAAACTC CTGGCCTCAA GTCATCCTTC TGCCTTGGAT 1080 TCCCAAAGTG CTGGAACTAC AGATGTGAGC CACTGCACCC AATGGCCCCC ATTAAGCTTT 1140 ATTTATTTAT TTATTTATTC GAGATGGAGT CTTGCTCTGT TGCCCAGGCT GGAGTGCTGT 1200 GGCACAATCT TGGCTCGCCG CAACCTCTGC 1230
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