Tag | Content |
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EnhancerAtlas ID | HS023-13288 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr19:45589380-45591430 |
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) |
Foxd3 | MA0041.1 | chr19:45590106-45590118 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr19:45590405-45590417 | GTTTGTTTGTTT | + | 6.32 | HES2 | MA0616.2 | chr19:45590246-45590256 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr19:45590246-45590256 | GGCACGTGCC | - | 6.02 | Nr2f6(var.2) | MA0728.1 | chr19:45590323-45590338 | TGAACTCTTGATCTC | - | 6.25 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr19 | 45590671 | 45590748 | chr19 | 45590753 | 45591181 | chr19 | 45589963 | 45590124 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I045087 | chr19 | 45590473 | 45592100 |
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Enhancer Sequence | TCCCAAAGTG CTGGTATTAC AGGCGTGAGC CACCACGCCC GGCCACACAA GAATCTCTTG 60 AACCTGGGAG GCGGAGGTTG CAGTGAGCCG AGGTGGCACC ACTGCACTCC GGCCTGGGTG 120 ACAGAGTGAG ACTCTGTCTC CAAAAAAGGA AAAAAAAGAA ACAGGACAAT TTCAATCACC 180 TCCCTTCTGT GCCTGGCCCC AGGGTCTTGG GTACCCAACA CTTGTCACTC AGCTCAGTTA 240 GTCCTCACTA GGTTTAGAGA GGAGAGGACC AAGCCACAGG GAGTGGTGCA GCTGCTAAAA 300 CCTAGGTCCT CCTCTCTCAG GTCTGCACCC ACAAGGCCAG CATTTCCCTA TACACATTCA 360 ACATCATAGC ATAGCGCTTC ATATGTCCCA GACATGTGCC AAACATGGTA GGTTAGTTAG 420 GTAATTTAGT CCCCATGCCC GCCCTGTGAG TTAGGGCTCT GTTTTACAGA TGGGGAAACA 480 GAGGCACAGA TTAGTCAAGC CATTTACCCC AGGTCACACA GCAATACTAA CAATAAGAGC 540 AGTTCACTAT TATGGAGAAC CTAGAATGTG CCAGGCCCTG TCTGGCAGGA GCCTGTTGAA 600 TCCTGATAAC AGCATAGGCA GCAATTGGGG CTATTTTTCC ATACAATGGA AGAGAAAACT 660 GTCTCTTACT GATGTCACAC AGCTAAACCG GCCTGGGATC TCCACTCTTC ATTCATTTTG 720 TTTTTTGTTT GTTTGTTTTT TTCGAGATGA GTCTTGCTCT GTCGCCCAGG CTGGAGTGCA 780 GTGGCGAGAT CTCCGCTTAC TGCAACCCCT GCCTCCCTGG TGCAAGCGAT TCTCCTGCCT 840 CAGCCTCATG AGTAGCTGGG ATTACAGGCA CGTGCCACCA TGCCCAGCTA ATTTTTGTAT 900 TCTTAGTAGA GACGGGGTTT CACCATGTTG ATCAGGCTGG TCTTGAACTC TTGATCTCGT 960 GATCCACCTG CTTTGGCCTC CCAAAGTGCT GGGATTACAG GCGTGAGCCA CCGCGCCCAG 1020 CCAATGTTTG TTTGTTTTTG AGATAGAGTA TTGCTCTGTT GCCCAGGCTG GAGTACAGTG 1080 GCACAATCTC TGCTCACTGC AACCTCTGCC TCCCAGGTTC AAGTGATTCT CATGCCTCAG 1140 GCTCCCCAAG TAGCTGGGAT TACAGGCACG CACCACCACG TCCGGCTGAT TTTTGTATTT 1200 TAGTACAGAC GGGGTTTTAC TATGTTGGCC AGGCTGCTCT CGAACTCCTG ACCTCTAGTG 1260 ATCCTCCAGC CTCAGCCCCT AAAGTGCTAG GATTATAGGC ATGCGCCGCC ATGCCCAGCT 1320 CATTCATGAA TTCTCATTGG TCTCTATGGC AGGCAGTTTC TGGGGGCTGG AGATCCAGCA 1380 GTGGGAAAAG CAAGGTGGCC ACCTTGAAAC TCACGGAGGG AAAGGAGATA CAGGCAGATA 1440 CAGGGAACCG AAAGTGCAAG AGCCCAAGAA GGGATTGCCA GGCATCGCGC CTGAGGATCA 1500 GCGAGGAGGC CTGTGTGGCT GGGGTGGGGA GAGCAAGCGT GGTACACCAC GAGGGTGCCG 1560 GCAGGATCCA GAGCTAAGAC AGAAGCCACA AGAGGGCTCC GAGCAGAGGA GGGATATGAT 1620 CTGACTCAGG CATTAACAGG GTGTTGGGGT GCAGACGGCG GGGGGTGAAG GTGGAAGCCA 1680 GGGACCCAGT GAGGAGTTGA CTACAGTACT CCAGGCAGGA AGTGTCTGTG GCTGCAGCAG 1740 GATGCTGGCA GTGGAGGAGG TGAGAAGTGT TAGGTTGTGA ATAAATAAAT ATGTGTGTGT 1800 GTGTATATAT AGATATATAA TTTTTTTTTT TTTTTTTTTT TGAGACAGAG TCTTGCTCTG 1860 TCGCCCAGGC TGGAGTACTG TGGCACAATC TCGGCTCACT GCAACCTCTG CTTCCCAAGT 1920 TCAAGTGACT CTCCTGCCTC GGCCTCCTGA GTAGCTGGGA TTACAGGTGC CCGCCACGAT 1980 GCTTGGCTAA TTTTTGTATT TTTCGTAGAG ACGGGGTTTC ACCATGTTGG CCAGGCTGGT 2040 CTCGAACTCC 2050
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