Tag | Content |
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EnhancerAtlas ID | HS151-11923 |
Organism | Homo sapiens |
Tissue/cell | OCI-LY1 |
Coordinate | chr8:141965520-141966880 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr8:141965672-141965693 | GAAATGAAAGAAAAAGTAACT | - | 6.64 | NFE2L1 | MA0089.2 | chr8:141965802-141965817 | AAATGACTCAGCAGG | + | 6.64 | Nfe2l2 | MA0150.2 | chr8:141965800-141965815 | GCAAATGACTCAGCA | + | 6.04 | REL | MA0101.1 | chr8:141966250-141966260 | GGGGATTTCC | + | 6.02 |
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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 |
GH08I140954 | chr8 | 141965060 | 141967499 |
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Enhancer Sequence | TCTCCCCAGC CATGTGGGAC TGTGAAGTCA ATTGAACCTC TTTCCTTTAT AAATTACCCA 60 GTCCCAAGTA TGTCTTTATT AGCAGTGTGA GAACAAACTA ATACAGACAT ATTAAAAAGA 120 TAAATTTAAA AACCAAACCC ACAGGACAGG GAGAAATGAA AGAAAAAGTA ACTGAATTTT 180 TGAAGCTATA AGAAAAGCCT CTAACACTGA AGATAGAAAC CGAACAAACA GGAAAACAGA 240 AAAACTTGGG GGAAATGAAC GATAAAAGAT CGGAAGCATA GCAAATGACT CAGCAGGCCC 300 AATGCAGCCA GACCAAGCCA GCAGCCAAAA ACACTAAGAA CCAATTCCAT TTCCACAGCC 360 ATGTCGGAAG AAGGTTCAGA ACTGGCAGCA CTAAATGCAG ACAGAACAAG GGGTAAAGAA 420 GGTGGAGGCA TAAAGGATGA TGGAGGTTAG GTGAAGACTA TCTACGATGC AGCTAAAGCC 480 TCAACACCAT GCCTTCGTGG GACTCCCCAA CCATGACAGA AGACTGGGGG CTCTCTGGAA 540 AAGGAGAGCA TCCTTAGACA GAAGTCACCC TGCCCAACTG TACAAAACAG AGGTCGATCT 600 AGTCACTGAA CACACATTTC AGCTCCTCCA CTACGCCCTA TGCACTTTCC TCTCAAACTT 660 CAGATAGTCA GGTCTTTACC CTGCAGGAAC CTGATACGTC TAAGAAGAAA GATCTAAAGA 720 TACCAATGCT GGGGATTTCC CAACAAATGG GCCATCCAGA ATATCCTGAT GCAAAAGTCA 780 GAGTCAAAAG GCTGAACCCA CTTGCTAAAG CTTCCAAAGA ATTTTTTATT CACCACAAGG 840 AAATTAATAC CAGACATGTG AGAAAATTCT GTAACACAAA AGACAGAGAA CAACACGGGA 900 GGGTGGGGAA GCGGGGAAGG AATAAAAAAG CCACTTGGGG GAAATAATAC ATTACTCACG 960 CGTTTTAGTG AAGCTGGGGA AAACAGACCT ACTGTGCTGC CAGTCGTATA AAAGTCTAGC 1020 ACATACGATT ATGTACAGTA CCTAACACTT GATAAACAAT TATGTTACTG GCTTATTTAT 1080 TGTGCACTTT TAATTATCAT TGTAGAGTAC ACGCCTTCTA CTTATTTAAA AAGGACAACT 1140 GTAAAACAGC TCAGGCAGGT CCTTTGGGAG GTATTCCAGA AGGCACTGTT AACCTAGGCG 1200 ATAACAGCTC CATGTGTGTT ATTGCCCCTA AAGACTTTCC AGTGGGACAA GATACAAAGG 1260 TGGAAGATAT TGATATTGAT GATCCTGACC TTGTGTGGGT CTACCCTAAT GTGTGTATTT 1320 GTGTCTTCAT TTTAACAAAA AAGTTTAAAA ACCTTAAATT 1360
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