Tag | Content |
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EnhancerAtlas ID | HS018-00261 | Organism | Homo sapiens | Tissue/cell | CD19+ | Coordinate | chr1:20497080-20498350 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MAX | MA0058.3 | chr1:20497856-20497866 | ACCACGTGCT | + | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH01I020171 | chr1 | 20497696 | 20498750 |
| Enhancer Sequence | AGAACCCAGA TCACCTCGCT CTCAGCCCTG CTCCTGGGGG CAGGGGCTTG GCAAGGTGGG 60 GGTGGGGATG ACAGGGGCTG GCCTGGTCCT CACGGGCTGG GTCAGCTGAG GAGGCGGGTG 120 CTGATGCCCT GGTACTGATG CGGAAGCCTC CTCCCACGCT AGTGCCCTGA GCAAGGCTCT 180 GGACTCAGGA GCCCTGGTCA AGGCTTCAGG AGCAACTGGC TGCTTCTGCT CTGAAGGGGC 240 AACGTGGGAA GAAAGTACAG CCCAGGCCAC GTACTTTCGG GTCCAACTCC CAGCCCTGGC 300 TGGCACCTCC CACCACTGCC CAGCAGTGCC ACTGCCTGGG GCTCCAGCCT CTGCTCCTCA 360 ACCTTTGCTC CACTCTCCCT CATCTCCTGG GGTCCTGGGC TGGGAGGGTG AAGAGCATTG 420 AATAGAGAAG CTTCCCTGGG TGCAGAGAGC CTAGGCCAGC CCTGGCGAGT GCAGCCAGCC 480 CACAGGAGCC CAGGGTGGAG GCTTGGGCTG GGCCAGCCAG GTGTCCCCAC CCCTGTGGCA 540 AAGACAGGTG GGAAGAGGCC ATGGGAAACT CGATCCCTGG AGGCCACCTT CTCCAGTCCC 600 CTCTCCCCAT CCCTCCCACC AGGCCCTGAT CCCTTCCCCT CTCCTGAACA TGGCCTTGGA 660 GGTGTCACAG AAAAGACACT TTGCTTTAGG CCTGAGAAGG ACCACACCAG AGAGCTCCAA 720 CTCAGGAAGT CTCCTTGAGC TCACGTGGGG AACAAAAGGG GGTTCTTTCC CTGTCAACCA 780 CGTGCTGGTG GCAGTGGGCA GGGCAGGCCA AGAGCTGAGG CAGGTCCTCC CGGTGCAGGG 840 GTCCGAGCCC CCAACCCACA CAGCTGGTGC CAGGGAGACC TCACAGTCCT AACTCTGGGT 900 ATTGGTGTGT GCTGAGCTGA AGTGGTGGGT TGGGGGAGCT CAGGAGACCA GGGTTCTGAG 960 CCCTGGAACC CACTACGGGA TGGAGGATGT ATCTCCCGCC ATAGGGGATG AGTGGCAGAG 1020 AGGTGGTAGT TCCCTGACCT CAGGAGGAAA CAGAGGAACT CCAAGGTGCA CTCACAGCTC 1080 TGAATAAATA CACCTGGGAA GGAAAGTGAT TCATGCAACC CCACGAGGCC AGGCAGGAAG 1140 TGAGCCACAC ACTATAAGAA GCCACTTCTT CTTTTTTTTT TTTTTTTTTT TTGAGACGGA 1200 GTCTCGCTCT GTGGCCCAGG CGGGAGTGCA GTGGCGCAAT CTCGGCTCAC TGCAAGCTCC 1260 GCCTCCCGGG 1270
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