Tag | Content |
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EnhancerAtlas ID | HS023-04836 | Organism | Homo sapiens | Tissue/cell | CD8+ | Coordinate | chr11:77703910-77705630 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SP8 | MA0747.1 | chr11:77705483-77705495 | AACACGCCCACT | + | 6.07 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CCTCCTCATC TTTTCAGCGG AGAAAAAAGA ACAGAAGCAC TAAGATCTCA TTTAATCACT 60 TTATGTTAAC AACTGATGAA AAATTAAGTG AAGAAATTAG CTCTTCCCTT AAAATTCTTA 120 GCCATTTCTA TCCTAGTCCT CTCAAACTCA GTTTTCAGTC TTATCGAAGC TGTAGTTAGG 180 TCAAAAGCTA GGAATTTTTT CCCTAAGTAT TATATAAGGG AGAGGACAAG CAATATCAAC 240 TGTCATTCAA CCACCAATAA CACTTTAGTG AGCCAGGCCC TATTGTCCAT CTCCAGGACA 300 CGGAGATGAG CCAGGCATTA GCTCTGCCAT CAAGGACCTC CGACTGGTGG GAAGATAGGT 360 ACACCGGTAA TGACAGCAGC ACTGAACAAA AAGTACAAAT AGATTAGTAC CACAGAATGC 420 TACAGAAACA GGTGAAGAAG AGACTAAGCT CTCGCTGAGG TTTCATTTGG GTCTTGAAGC 480 ACAAATGTTA AGTCCACTGG GTGGAGAACA AAAAGAAAGG GAAGAATGGC ATGTATTCTG 540 TGAGAAGAGA CAACCAGTGC AAGAGTTTTG AGATATGCAA ACACAAGAAC ACATGGCATA 600 TCTGGTCATG TGAGGATGGG TGGAAGAGGG CTGAGCAGTC TTGGGAAATG GGAACAACAG 660 AATGTTGGGA AGAGAGGAAA TCACATTGTG CAACAGTGCT AATGTTCTTA ATGCCACTGA 720 ACTTTATACT TAAAATTGTT AAAATTGTAA ATTTTATATT ATGTATTGAC ATATTTTGTA 780 TTTGTATTAA CATATTTTAA TGCTGGATGA ATGAATCCAT GTAATGTTTA AGGATCAGTA 840 TCCTGCTGGA TGCTCTAAGC CTTGCCACTC TACAAGTCTA AGGATCTAAG AATGCAACCA 900 ATGCACTGGT GTAAATTTGG GGGCATGTCA GGAATGCAGA ATCTTGCCTC ACCTCCTCTG 960 CTTGACTTAT CAAATAGAAT CGACATTTGA ACAACGTCCC CAGGTAATTT GTATACACAT 1020 TAATATCTGA GAAATAGGAC ATCAGGATGA TTTAGGATCA ACCCTAGCAA CATCTACGTG 1080 GAGACACATG GAGCATCACT GACTCCCGAC AGGGACTCTG CCCACCTGTC ACAACTTCAT 1140 GGTGAGGAAG GTACTGCCCT CCTTCCTAGG TGAGCTGTTC TACCAATAGA GAGCTCTTCC 1200 CCTATGAAGT CTGTGACCCC CGCCTGCTTA GACTGCGCCT GAAGGAATTC TATAGACCCT 1260 TCTTTCAGCC CCTTAGAACC TTGTGTATAT TCCAACTGGT CCCTGGGAGG TTTTTTTTTG 1320 GAACGGGGGT GCGGGGAGGC TAGAAGGGGC TCTGCTGCTA ACTGGCTGTA TCCTCGTACC 1380 CCTCCGGAAG GCTCAATGTC CACATCTGGA AAACGAGGAT GCTAATGTAA CGCGATGGAG 1440 CAAAGTTGTG TGAGAGAATA AAATGAAATA ACGGATAAGA CAGTTTCGTA AATTAAAAAA 1500 CACTGTTTCT CCTAATAATT TTTTTAAAAT CCTGTCAGAC TTCACATATT AATGACAACA 1560 GCGGCTGCAA ACTAACACGC CCACTAACTT GCAATATCAG AGATTATCAA CAAGTCAGCA 1620 CTTAACACGG GCGTATGGAG CCTCTTCTGT TCCGGCAAAG TGCCTGGGAT TTGGATAATC 1680 TACCCTGGTC CGGATCGGTT CTGGATCTTT CCCGCCAGAG 1720
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