Tag | Content |
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EnhancerAtlas ID | HS019-02327 |
Organism | Homo sapiens |
Tissue/cell | CD20+ |
Coordinate | chr10:100013550-100014680 |
Target genes | |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXA1 | MA0148.4 | chr10:100013933-100013949 | GCCTAAGTAAACATGC | + | 6.01 | FOXC1 | MA0032.2 | chr10:100013936-100013947 | TAAGTAAACAT | + | 6.02 | Foxa2 | MA0047.2 | chr10:100013934-100013946 | CCTAAGTAAACA | - | 7.22 |
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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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Enhancer Sequence | CACCTGGGGC GGCGGAGGGC ATGGCAGTGA CTCAAAGGGT GGAAAGGCAG CCAGTCTTAG 60 TCTCCAGCAC AGAGGGCAAG CTTGCCCCCA GATTAAACCC TCCGAGAGGA CCCCACAAAA 120 GAAGGGCAGT TTTAAGAGTC AGGAGATGGT GAGTTCTAAT AACATTTAAA GGAAGTCTAT 180 CACCTTAACC TGGGAGGCAG CTACAGTGTC ATGGTTAGGC TTGCTGGTTT TGGAGCCAGG 240 CCACCTGGGT TCATTCTTGG CTTACTTTCT GACTGTATAA TTCACTAGCT CTATAACTGC 300 TTAACCATTT TGTCTCTCAT TTTCATCATC TGTAAGATGA AGATAATGGT GATATTAATC 360 TGATGACACC TGTAACATGT CTGGCCTAAG TAAACATGCA GTTGAAGCTA GTATTTATTT 420 TGTAAAATGC TTTTAAGCCT GTAAAGTGCC TTTATGTAGC TTAGTTCATA TAATCCTCTC 480 AAAAAGCTCT GCTGATACCT AACCTGGATA CTTTGCCTGT ACTGTCACTA AAAATCACTA 540 TCACTAAAGT AGTCCTGGGC GGAAGTGAGG CCCTGCCACA CCACTGACCA CAGCATGCAT 600 GCCACCTGGG CAGGCCGGCC GCAGCTTGCC CCAGGCTGGA GCCATCTGCA TCTGGCAGTT 660 GGCCATGTAG GGTCCTGTGG TATATATTGG AGAGAGCCAG GAAGTGCCCA CTGACAAACC 720 TAGAGTTTCT TGGTGAAAGA AGGCGAGCTT TCAGAGAGAA TGAGAAGAGA GAGTAAAGGA 780 AAGAAAGCAA TGTGAAAAGC CAGGGAGGAA AAACAGGTGG TTACAGAGAC TGCAGATTGG 840 CTGACTGTGC CAAGTTGTCG TGAAGGATCA AATGTGTTCA AGAAGAGCGC TCCCACTGTA 900 GGCAGTGGAG CAGGGAGGGG TTCGAGGTTC CCAGGAAGGG GAGTCAAGTG AGGAGCAGGC 960 TCCCCACGTG CTGGGAGGCC TTGGTGATGG GGAGGTCCAC TCTCATGCCC CATCCCTGCA 1020 GGGGAGGGTC TGATGGATGG GCCCAGTGTT CTCCCCAGGG TGCCCTGGAC AGAGAGGAAG 1080 CCAGGAGCTC ACTGACAAAG ATGAAGGATA TCTTGGTGTC GAAATTTGGC 1130
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