Tag | Content |
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EnhancerAtlas ID | HS022-02662 | Organism | Homo sapiens | Tissue/cell | CD4+ | Coordinate | chr11:66437920-66439460 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Sox6 | MA0515.1 | chr11:66438720-66438730 | CCATTGTTTT | + | 6.02 | Stat4 | MA0518.1 | chr11:66437944-66437958 | CTTCCAGGAAATGA | + | 7.38 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ACAAATGGGC CACATCCATT TTGGCTTCCA GGAAATGACC AGCACTGAGG AACAGCTAAG 60 AGAAGAAAAC AATCTTTGCC CAGGGATTGT GAACCACCAA ACCCATGGAC CCTTACTGAT 120 GAAAGCATCT GAAGTCTTTA AAAGCAGTTA AAGAAAAGGA GTATTCCTGG CATTATTTAG 180 TCCCAGGTTG CACAAGACTC TCCTGGAGAT CAAGTCAGTG CTTTCCAAAT TGTAGCCAAA 240 AGAAAATGCA CGGGAGGCTG AGGCAGAAGA ATCGCTTGAA CCTGGGAGGT GGAGGTTGCA 300 GTGAGTGGAG ATCATACCAC TGCAATCCTG CCTGGGCAAC AGTGTGAGAC TCCATCTCAA 360 AAAAAAAAAA AAAATGGAAA ACGCAGTCAG TACAGATAAA AAGAACAGGG CTTCTCATTA 420 CTCTTAAGGA CTGCTGAGAA CAAATCCCCC CTCTGCAATC AGCAAGTTGC TCTCTCTTTA 480 ACAGACCTTC TTCTGGATGC AGCTATGCGA GAGGAAGCCT TGTGCTCCAC CATCCTGTTG 540 GAAATAGCCC TATTGAGGAC GGCAGCCAGA ACAGTGCCAT GCACTGACCC TGAGAGGGGA 600 GCGGGTTAGT GTGGCAATAT CACTTTAGTC AAATTCCTTC TGCCCAATGT CAAAGAGTCC 660 TATCACTCCA GTTTCTAGCA GAAACAAAAG TGCTCAGGCT TTATACCTCC AACTGCTAGG 720 AGACAGGCCG CATCCACTAT CACCAATAGA GTCAGCAGAT ACCCAAAATG GCACTAAATC 780 TCTAAAAGCA TTTTGCCATC CCATTGTTTT CAGAGATTTA AATGCTCCTA ATTGTTAGAT 840 GTTAGGGGCC ACAATGCTAA CTGTGCTTTG AACAGAAACA CAGATTTCTG CCACAATTTA 900 TATCTCAAAT GCATAGTTCC CTATAATTTA GACTAAAAGA TTATAAATGA CTTGGCTTTC 960 AAATATACAT GGTGACATTA AGCTATGTGA CAGACACAAA GTATACTCCA ATTGTGAAGT 1020 CAGAGTGACC ATGACAGTCT AAAAAGGAGC CAATCCAGAG ACCTAAAAGT AACATTTTTA 1080 ACAAAAAAAT TCAATTAAAT TTGCACTTTA CTTTTATAGA TTCTGGGTCC ATTTTTTGGA 1140 GAAACAAAAC CCAGCAATTT TACCTTGATG TTTTTTAACT AAATCCAATC TTCATTCCTG 1200 CTTTTATTTA GAGGGTGGGA AATCAAGTTT ATCTGTGGTA AAATCTACCT CTGTGTAGTT 1260 GTGAAAAGGA TGCAGGTATC AATTTTTTTG TTGCGTTTGT TTGATTTTTG AGACGTAGTT 1320 TTGCTCTGTC GCCCAGGCTG GAGTGCAGTG GCGAAATCTC GGCTCACTGC AACCTCCACC 1380 TCGCGGGTTC AAGCAATTCC CTGCCTCAGC CTCCCGAGTA GCTGAGATTA CAGGCACCTG 1440 CCACCATTGG TGTGGTTTTA AAGCAATTTT TGTATTTTTA GCAGAGATGG GGTTTCACCA 1500 TCTTGGCCAG GCTAGTCTTG AACTCCTGAC TTCGTGATCC 1540
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