Tag | Content |
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EnhancerAtlas ID | HS150-10184 |
Organism | Homo sapiens |
Tissue/cell | NT2-D1 |
Coordinate | chr7:101907550-101908450 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr7:101908419-101908434 | GAGGTCAGGAGTTCA | + | 6.22 | SPIC | MA0687.1 | chr7:101907887-101907901 | GGAAACAGGAAGTA | + | 6.29 |
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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 |
GH07I102264 | chr7 | 101907654 | 101908287 |
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Enhancer Sequence | GCTGGGATTA CAGGCATGAG CCATCGCGCC CAGCCCAGAA GTTAACTTCT AAACAGTACT 60 GGCAGAGCTG AGGGAACGAG CCCTGCAGAT GTGAGAAGGA AGGACGTTCT AGGCAGTGAG 120 AACTGCCAGT TCAAAGGTCT CGTGGTGCAA ATGTCTCTGG AAACCAGCAT GGCCGCAGCA 180 CCGTGACCAG GAGGAAGAGT GGGAGGCGAT GAGGTCAGAG AGACCAAGGA GAGGCGGAGC 240 ATGGGGGCCT TGTCGGCTAT TGCTGAGGCT TTGTTTTTTA CTCTGAGTCA ACTGGGAGGC 300 ATTGGACGGT TTGAACAGAG GGTCCTGGCT CTGGTGGGGA AACAGGAAGT AGGATTCATT 360 GGTAGGAGTG AGTAAGGAGG GGTCAGCACA GGGGAAGCCC TCAGAAGCTC ACCCAGGAGG 420 CCACAACTGG GGCTGCGTTT AACCCCCACA GCCATGCCAG ATGAGCTGCT TCTCAGCCAC 480 CACGTGGGAT CGATTTCTTC CACATTGAAC TTGGTCAAGG CCCGCTGCTT TGTGCTGTGG 540 ATCTTCTGGC AGCCAGGGAA CTTAGACTTG GCCCTGCATA TGGCCTCAAT CACACCCTCA 600 TGGTTCTGCT CTTAGTACGG ATAGACACAA TGACCTGGCC AACATAAACC CTGGCTGTCA 660 CACCCTGGGG CTTTCCAAGG GCACCCCGAA TACTTGCCTG GTGCCTAGAC CACAGACAGC 720 ACGAGGTCAG AGACACAAAT GTCCAGTGGA AAGAATTGTC TCCAACGTTC CTTAGGGCAA 780 CCCATGTAAG AAACAGACTG TGTGGCCGGG GGTGGTGGCT CACGCCTATA ATCCCAGCAC 840 TTTGGGAGGC CAAGGTGGGT GGATCACCTG AGGTCAGGAG TTCAAGACCA GCCTGGCCAA 900
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