Tag | Content |
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EnhancerAtlas ID | HS018-16968 |
Organism | Homo sapiens |
Tissue/cell | CD19+ |
Coordinate | chr3:195116050-195116990 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2B | MA0660.1 | chr3:195116190-195116202 | GCTAAAAATAGT | + | 6.11 | MEF2C | MA0497.1 | chr3:195116188-195116203 | AAGCTAAAAATAGTT | + | 6.29 | NEUROD2 | MA0668.1 | chr3:195116388-195116398 | ACCATATGGC | - | 6.02 | Nr2f6(var.2) | MA0728.1 | chr3:195116763-195116778 | AAGGTCAGGAGTTCA | + | 6.04 |
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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 |
GH03I195396 | chr3 | 195116730 | 195116929 |
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Enhancer Sequence | AACAGAGAAT AAGTAATAAG GGAGATAGAT GTTAAGAGAA AGGGAAGAAA AGAGAAGACA 60 ATGAGCACAG TCACAAAGGT CAGCAAACAA TTACCCAACA GGCAAGTTTG ACCCATAACC 120 TGTTTTTACA AAGTCTATAA GCTAAAAATA GTTCTTACAT TTTTAAGTGG CTGAAAAATA 180 TTTTTAAAAA ATAATATTTT GTGATGCATG AAAATTATAT TAAACTCAAA TTTCTGTTCC 240 TCTAAAGTTT TACGGAAGCA GAGACAAGTT AATTCACTTC CGTAGTCTCT ATGGCAGCTT 300 CCACGCCATG ATGGCGTAGT TGAGTAGCTG CAAGAGAGAC CATATGGCCC ACAAAGCATA 360 AAATATTTAC TATCTGGCCC TTTACAGAAA GTTTACTGAC CATTAAGAAT GTCAAATATA 420 AGAACATGAA TGAAAATCTT TTCTCATATA TGAAATACAT AAAAGAAAAT AAAATTTGGA 480 CTTAGCTCTA GCAGTCTGTA CTCTAAGAAG CTGAATAAGC CCAGAATTCA GAAAAACAGA 540 TACTTTATTT TTAATAACAA TACCTTCATT CTCTTATCTA TTCATGCATC ATAGTTTTTT 600 ATTATCAATT GAAAAATAGT TACCTAAAAA CATAAAACTA GAAGAGAAGC TGGGTGTGGT 660 GGCTCATGCC TGTAATCCCA GCACTTTGGG AGGCTGAAGT GGGTGGATCA CATAAGGTCA 720 GGAGTTCAAG ACCAGCCCAG CCAACATGGT GAAACCCCTT CTCTAATAAA AATATGAACA 780 TTAGCCAGGC GTGGTGGCAG GCACCTGTAA TCCCAGCTAC TAGGGAGGCT GAGGCAGGAG 840 AATCACTTGA ACCCAGGAGG TGGAGATTGC AGTGAGCTGA GATCGCGCCA CTGCACTCCA 900 GCCTGGGACA CAAGAGCAAA ACTCCATCTC AAAAAAAAAC 940
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