Tag | Content |
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EnhancerAtlas ID | HS018-00464 | Organism | Homo sapiens | Tissue/cell | CD19+ | Coordinate | chr1:32313600-32315270 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr1:32313808-32313829 | GGGGGAGGGAGAGAGGGGGAC | + | 6.64 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 32313927 | 32314685 | chr1 | 32314121 | 32314597 |
| | Number: 1 | ID | Chromosome | Start | End |
GH01I031845 | chr1 | 32310997 | 32315950 |
| Enhancer Sequence | AGGCGGAGGT TGCAGTGAGC CAAGATTCCA CCACTGCACT CCGGCCTGGG TGACAGAGCG 60 AGACTCCATC AAAAAAGAAA AGAAAAAGAA AACTATTGTG AAGGAGGAGG AGGTGTGCAA 120 AAAGCAATGG AGTTAGAGGC AGGTGGAGGG TGGGGCCAGG ACCGAGACAG AAGTGGGGCC 180 AGGGGTAGGG AAACTGGTAC AGAGGTCGGG GGGAGGGAGA GAGGGGGACA CTGAGGCAGA 240 CAGAGAGATG GGAAAAGTGA GACCAAGAGA AGCAGAGGTG AGAAATAGGG AGAGACAGAG 300 ACCAGGACAA GGGCAGGGGC CCGTGGAGGA GGCCACCTCC ATGGTACTCC CTTCAGGACC 360 TCAACACCCC ATCAACCTCT CGAGACCCCT GTAAGATCCA CGGGCCCAGG TGCCTGATCT 420 AGGCAGCCCA GCAATGGCCC ATCCTCCAGC CCCACTCCAG CATCTCAGGG TCTGGGAACT 480 CAGGAGCCAT CGGTGCTGCT TGGATGACCT TAAGCAGGGA AGTGGCATGA CCAAGCTCAA 540 GTGTCACAGA GCCCCTGTCT GCGAGGAGGA AATGGGTTGG GTCCAGGAAA ACCACTCTGA 600 GAAATATCGG GTACTTCTAA GAGCAAGGCA GGGCTACAAA GCGCTTTCAT ATCACCTGCG 660 CGCACACACA TGTGTGCACA CACGCACACC CACACGTCTT GGGGGGGGGG GCACACATTC 720 GTTACAGCCC ACACAGAGAA ATTCCAGTAT GTGGTAAGGG CCAGAGCTCT TACATCTGCT 780 GGAGGCAGCC AGCAAGGCCA GAAGTGCACC TGCAGCAGGA ACTCATCTGC TGAGACACTG 840 TACAGACCCT GGTGGGGCGC TCCTCACACC TGCTTGGCCC AGTTGACTCA GGGCATCCAG 900 GGGGGACAGT TGCATGCACC CTGCTTGAAC CCCATTTCAA ATGCGCCCTG CAGCTTCCCT 960 CAGCTTTTCT GCCTCCGGGC TTTCTCCTTA GCTGCAGAAG GCCACTCAAC CCTCCAGCAG 1020 ACACAGCTTG GAAGTCCAGG AAGCTGATGT CCCTGCGGCA GCCCTCAGCA ATGAGGGACT 1080 GGAATCATGG ATAAATGCGT CAGCTTTCCT ACCTTCTGTG GAACAATTCT GAGGGTATTC 1140 CTCATGGTTT CTCTGAGGGG CCCCAGCAGG ATATGCCCAG TTGCCTACAG TGGGAACCAG 1200 CTCAGAGAAC ACCCTCGTTG AAGGAATCAT TGGTCCTGTG GAGCCCCACG GCCTGGGTGT 1260 GTCTACTTGC CTCTTTGCGG TATCATTTAC TTGCTTCTCC ATCCCCTATA TTTCCTGTAG 1320 ATAGAAGTCC GGCCTCAGGT TCAACTCTTC TGGCAAGGCA CCAGAGCAGG CACTGTTGGT 1380 GTCCCACCAT GTCCCATGGG CCAGTGCTGG AGGCCACCTG CAGACCTTCT GAGTCTTGCA 1440 ACCTGAGGGC ATTTTCTGCT CCTGAGAAGA GCCAGGGAGT TAACAACCCC GAGCAGCCTT 1500 TGACTAGCGT TGGGTGGAGA TTGGTGGCTA AATAGCCCAG CTTCCTCGCC TCTCTAGGGA 1560 AGGTTTCCGA CATGTTCTGT ATAGCCTTTC AGAGGGTCCC CAGAGGAATG GAGCTCCAGT 1620 TCCCGGAGTA AAGACCCACT CATTAATTCA CTTTTTATTG GCTTTCTGCC 1670
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