Tag | Content |
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EnhancerAtlas ID | HS062-00628 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr1:62640910-62641950 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr1:62641425-62641444 | TAGCCAGAAGATGGCGCAG | + | 6.42 | Nr2f6(var.2) | MA0728.1 | chr1:62641766-62641781 | GAGGTCAGGAGTTCA | + | 6.22 |
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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 |
GH01I062175 | chr1 | 62641361 | 62641570 |
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Enhancer Sequence | CTCCTATTTC AGTGTCCCTA GTAGCTGGGA CTACAGGCAT GCCACTATGC CCAACTAACT 60 TATTTATTGT AGAGATGGGG TCTCACTATG TTACCCAGGC TGGTCTCAAA CTACTGGCCT 120 CAAGTGATCC TCCTGCCTTG GGCTCTCAAA GTGCTGGGAG TATGGGCATG AGCTACCCCA 180 CCTGGACAAC TGAGCTGTTT TAATCTGGAG AGTTTTGTGA TCAGATTTTC CCTTTAATGA 240 AATGAAGTTT TGGCCTTCAC TGCAACATTT TTACTGTTTC TCAGAGTGTG GCCCATGAAC 300 AGTTTACATC AGAACCCTGG ATCGCTGCAG GTATACATGT ACAAATCAGA GTCTGTATTT 360 CAACCTAGTT TCTTCCCTGA TTCGTCACTG AACACGCACA GGCGTACATA CTCTAAAGTT 420 CTTTGAAGAA CCTCCAATTT AACAGCTAGA AAAGCAGAGG AAAACCTGTA TCTAATATTA 480 AAGAACAATG ACTCTTCAGA AAGCTACTCA CATCTTAGCC AGAAGATGGC GCAGGTTTTC 540 CATTTACCTG GCTCCTGCCT GGCTAGAAAG ATGGAAATCT TGTTCAAAAG AAATTGCTTG 600 ATCTCATTAC TTAAGTCAGA AGAGGGCTCC CCAGAAATTA TGATGGCAAG TGAGAAATGA 660 GAAAGACTTA TAACAGGTGG GAATAGGCAT CCCATCTCCA TAGATGCCAC CCTTCTCTCC 720 AGAAAGCATA GCAAATTAGG ACATGTCCAC AAGGCTAGAA GAGTACTACA CTCCCAAAAA 780 GAAAGCTCTA AGCATCAGGT GCGGTGGCTC ACGCCTGTAG TCTCAGCACT TTGGGAGGCT 840 GAGGTGGGCG GATCAGGAGG TCAGGAGTTC AAGACCAGCC TGGCCAACAT GGTGAAACTC 900 CGTCTCTACT AAAAGTACAA AAATTAGCCG GGCATGTTGG CAGGTGCCTG TAATCCCAGC 960 TACTCAGGAG ACTGAGGCAG GAATGAAACT GGGAGGTGGA GGTTGCAGTG AGCTGAGATT 1020 GTGCCACTAC ACTCCAGCCT 1040
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