Tag | Content |
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EnhancerAtlas ID | HS022-13249 | Organism | Homo sapiens | Tissue/cell | CD4+ | Coordinate | chr8:28493600-28495150 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr8:28494553-28494571 | GGAAGGGAGGAAGGAAAC | + | 7.66 | Nr2f6(var.2) | MA0728.1 | chr8:28493631-28493646 | GAGGTCAGGAGTTCA | + | 6.22 | ZNF263 | MA0528.1 | chr8:28494539-28494560 | GAGGGAGGGAGCGGGGAAGGG | + | 6.34 | ZNF263 | MA0528.1 | chr8:28494543-28494564 | GAGGGAGCGGGGAAGGGAGGA | + | 6.62 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ACTTTGGGAG GCTGAGGCGG GTAGATCACA TGAGGTCAGG AGTTCAAGAC CACCCTGGGC 60 AACACGGTGA AACCCTGTCT CTACTAAAAT ACAAAAAAAT TAGCTGGGTG TGGTGGTGCG 120 CACCTGTAGT CCCAGCTGCT TGGGTGGCTG AGGCAGGAGA ATTGCCTGAA CCCAGGAGGC 180 GGAGGTTGCA GTGAGCCGAG ATCGCGCGAC TGCACTCCAG CCTGGGTGAC AGACCAAGAC 240 TCCATCTCAA AAAAAAAAAA AAACAAATGT CTAACTCGCC AGGAGACAAG ATCTTTCAAG 300 TACAGATATC TCACATGAGC TCTTATCACC CTCAACGGAA TCTTGTCACA GGACAAGGAA 360 GGATTGGGGC TGGAAGGATC TTACCTAATA GCCTCTTGGT ATCTGCTCTC TCCAAGGGCA 420 ATATCTGCCC TTAAGAGAAT TGTTGTCTGT AACTTTGATC TCAACTGGGT GATTGCTGAG 480 CTCTCAAGAC CTTTATCTTA CAAGCACAGT TTGAGTTGGT TTTTTCATGC TCTCACTCTA 540 GCCTAGGAAT CCTTTCGGCC ACTTTGGGCC TGTTGTGAGT TCCTAGGGTG GCAGATCTCC 600 ATGAACTTGC CCGTTTACTC TGCGGAAAAC TTAGTGTTAT AGCAGGTTGG CGCGTGGTGG 660 CTTACGCCTG TAACCCCAGC ACTTTGGGAG GCTGAGACAG GTGGATCACC TGAGGTCAGG 720 AATTCGAGAC CAGCCTGGCC AACATGGTGA AACCCTGTCT CTACTAAAAA TACAAAAATT 780 AGCTGGGCAT GGTGGCATGT GCCTGTAATC CCGGCTTGAA CCCAGGAGGC AGAGGTTGCA 840 GTAAGCTGAG ATCCCGCCAT TGCACTCTAG CCTGGGCAAC AGAGTGAGAC TGTCTCAGAA 900 AAAGAAAGAA AGAAGCGGGT GGAGGGGGTG GGGCGGGGAG AGGGAGGGAG CGGGGAAGGG 960 AGGAAGGAAA CATAGTGTTA TATCAGCCAA CCTAAAAGTT CCTCTTTCAG GTCATTAATG 1020 AAAAATATCC CAGTAATAAC ATTCCTTTAT AAAAGAAACC TTTTATAAAT CAGTCGTTTT 1080 ATTGTAATCA AACTTCTAGA TTCCATTCTT TCTGAACAGG TTCTGGTAAA ATGGGAACGG 1140 TTTCTATTAA TCAACTGGAC TCTCCTAGCT TAGTCGATTT TCTAGCCAGC TTTCTCTCTC 1200 TCCTGTTCTC CGCAGCAGAT TTTCAAACAC CGCATTCCCC TTAAACCTCC CAGGCTCCCA 1260 TCACTCCCAG CAAAGAGCCA GCCCGCTACT TTATGGAGAC AGGAGAGACT GTCAGACAGT 1320 TCCTGCTGCT GCCCAGGTGC ATCTGAGTAA GTTTTTCTCT CTTTCTATCC CATTCCAGCT 1380 GAAGAAGTAT CACTCCTTTG ATTAGGGCCA ACCTTTAAAT CTGTCGATTG AGTCAGTATG 1440 ATAGTGGCCT GTGTCTATAA TCCCAGCTAC TCAGGAGGCT GAGGTGGGAG GATCACTTGA 1500 GCCCAGGAGT TTGAGACCAG ACTAGGCAAC ATAGCAAGAC CCCATGTCTG 1550
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