Tag | Content |
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EnhancerAtlas ID | HS145-11477 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr19:6800820-6802030 |
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) |
POU2F2 | MA0507.1 | chr19:6801934-6801947 | CTGATTTGCATAT | + | 6.5 | POU4F2 | MA0683.1 | chr19:6801069-6801085 | ATCATCAATTATTCAC | - | 6.42 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_17561 | chr19:6798623-6803806 | CD4p_CD25-_CD45RAp_Naive | SE_18804 | chr19:6799714-6804369 | CD4p_CD25-_Il17-_PMAstim_Th |
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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 |
GH19I006799 | chr19 | 6799599 | 6804367 |
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Enhancer Sequence | GCAGTCGGGG TTTCACCATG TTGCCCAGGC TGGTCTTGAA CCCCTGACCT CAAGTGATCC 60 GCCCGCCTCA GCCTCCCAAA GTGCTGGGAT TACAGGCGTG AGCCACCGCA CCCAGCCGCT 120 CACCATCTCT TTGTCGCCTG CATGGCACCA TTCTCTCCTG TACCACCCCA AAGCCTTACC 180 AGGTGCCTCC TGCATTTAAC CAGGTCCCAT AGCTCTCTGT GCTTCCCGGC ACACCCTCTC 240 ACCACCCTCA TCATCAATTA TTCACCTTGC TGACTGCTTA GTGTTTGTCT CCTGGCTGGA 300 TTACATAAGC CCTGTAAGGG CAGAGCTCTG TTTGTCTTGA TCACCATTAG GTTCTGGTGC 360 TTGGCATACA GTAGGCATTC CACACATGCT TGCTGAATTA ATGCATGACC GGGTCTGGGG 420 TGCTGGGTTT CACACCAGGC TCTACCGCAA ACATTGGGTC AAGTATTTTC ATTCCCGACG 480 TACAGATGAG TCAATTGAAT CAACGGAAAG CAAAATGATC CCATCCAAGC TCCCTCAACT 540 TGCCGGGCTG GTCTGGGAGT CGAACCAGAT CTGCCTGACC CTCCCACCGG TGCTGAAAAG 600 TGGAGTGTGT GCTGGGGTGG TAGGGGATGG GGCAGAAGAG AGACGGGCTT CCTCACAGAA 660 GGGTTTGAGG GCTAGGATGA GGCGTGCACA CTCTGCACCC CTGCTTCGGA GCTTTGAAAG 720 GGTGCACAGC ACACCCGCCC TCTCTGGGAA CCCTCGGGAG CTTGAGGTTG CCTGATGAAG 780 GGGCTGATGG GTTGAACGCA AAGGGCCCCT CCACCCACCC TTTTTTCTAT CTCCCCAACC 840 AAGCCCTGGT AACAGGCATT TCCGGTTTCC GGCCGGCTCC CTGGTGCTGG GGTGGGGGTG 900 GGGAGTTGAT TGCTGCCGTC GTGCTTGGCT CTGGGTCCCC TTCTCCCAGA CCCCAGAGGC 960 CTCTGTCCCT GCACACTGCT TCCCCGAAGG AGCGTGGAAA GCCAGCCGAC CTTTCTGGCT 1020 CTTTCTTCAT CTTGGGCAGG GGTTTTGTTG ATGGGAGGCT GGCTGGCAAA TGGGGAAGAA 1080 TGAACCTCAG GGTTCACCGC AGTGCGCCTG GGTGCTGATT TGCATATGGG CACGATGCCA 1140 GCACAGTGGG TGCCCGCCTC TTCCTGGAGG AAGGAAGAGG GGCACTGAGG GGGGTTGCCC 1200 CCAGCAGGGA 1210
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