Tag | Content |
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EnhancerAtlas ID | HS182-08861 | Organism | Homo sapiens | Tissue/cell | Spleen | Coordinate | chr17:1286740-1287720 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HES2 | MA0616.2 | chr17:1286824-1286834 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr17:1286824-1286834 | GGCACGTGCC | - | 6.02 | Nr2f6(var.2) | MA0728.1 | chr17:1286900-1286915 | TGAACTCCTGACCTC | - | 6.22 | Nr2f6(var.2) | MA0728.1 | chr17:1287281-1287296 | AAGGTCAAGAGTTCA | + | 7.36 | RARA | MA0729.1 | chr17:1287281-1287299 | AAGGTCAAGAGTTCAAGA | + | 6.24 | Zfx | MA0146.2 | chr17:1286925-1286939 | CCCGCCTCGGCCTC | + | 6.01 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 1286983 | 1287040 | chr17 | 1287615 | 1287665 |
| Enhancer Sequence | GCACAATTTC AGCTCCTGGC AACCTCTACC TCCCGGGTTC AAGCAATTCT CCTGTCTCAG 60 CCCCTACCAG AAGATGGGAT TACAGGCACG TGCCACCACG CCCGGCAAGT TTTTGTATTT 120 TTAGTAGAGA TGGGTTTCGC CATGTTGGCC AGGCTGGTCT TGAACTCCTG ACCTCAGGTG 180 ATCCACCCGC CTCGGCCTCC CAAAGTACTA GGATTACAGG TGTGAGCCAC TGCACCCGGC 240 CCTTGTTTAA ACAATTTTTT AAAACACAAG TTTTTAGTTA AATTTTGTGC TGCACAATCG 300 TAAGTTGCTA GTATTATAAA CAGTTAATAA ACCTTTTCAG AAAATAGAGT ATTCCCGCAA 360 TCTCCGCACT TTGGGAGGCT GAGGTGGGAA GATTTCCTGA GCCCAAGAGT TCAAGACCGG 420 CCTGGGCAAT ATGGCAAGAC CCCATCTCTT CACACATTTA AAAAATTAGC CGAAGAGGGC 480 TGGGCACAGT GGCTCACGCC TGTAATTCAA GCACTTTGGG AGGCCGAGGC ACGTGGATCA 540 CAAGGTCAAG AGTTCAAGAC CAACCTGGCC AACATGGTGA AACCCCATTT CTACTAAAAA 600 TACAAAACAA TTAGCCACGC GTTAAGCAGG TGCCTGTAAT CCCAGCCACT CGGGAAGATG 660 AGGCAGAGAA CTGCTTGAAC CCAGGAGGCG AAAGCTGCAG TGAGCCAAGA TCCAGCCACT 720 GCTCTCCAGC ATGGGAGAAA GAGCAAGACC CTGTCTCAAA AAAATAAAAA TAAAAAATAA 780 ATTAGCCAGG CATGGTGGGC ACACCTGTAG TCCCAGCTAC CCAGGACGCA GAGGTGGGAG 840 GATTGCTTGA GCCCAGGAGG TGAGGGCTGC AGTGAGGTGT GTCTGCTACT GCACACCAGC 900 TTGGGCAAGA GTGAGACCAC ATCTCAAAAC ATTAAGAGTA CACATGTAAA AAGATTTATG 960 CTCGACCGGG CGCGGTGGCT 980
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