Tag | Content |
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EnhancerAtlas ID | HS089-06437 |
Organism | Homo sapiens |
Tissue/cell | Hela |
Coordinate | chr19:6800990-6801970 |
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 | AAGCCTTACC AGGTGCCTCC TGCATTTAAC CAGGTCCCAT AGCTCTCTGT GCTTCCCGGC 60 ACACCCTCTC ACCACCCTCA TCATCAATTA TTCACCTTGC TGACTGCTTA GTGTTTGTCT 120 CCTGGCTGGA TTACATAAGC CCTGTAAGGG CAGAGCTCTG TTTGTCTTGA TCACCATTAG 180 GTTCTGGTGC TTGGCATACA GTAGGCATTC CACACATGCT TGCTGAATTA ATGCATGACC 240 GGGTCTGGGG TGCTGGGTTT CACACCAGGC TCTACCGCAA ACATTGGGTC AAGTATTTTC 300 ATTCCCGACG TACAGATGAG TCAATTGAAT CAACGGAAAG CAAAATGATC CCATCCAAGC 360 TCCCTCAACT TGCCGGGCTG GTCTGGGAGT CGAACCAGAT CTGCCTGACC CTCCCACCGG 420 TGCTGAAAAG TGGAGTGTGT GCTGGGGTGG TAGGGGATGG GGCAGAAGAG AGACGGGCTT 480 CCTCACAGAA GGGTTTGAGG GCTAGGATGA GGCGTGCACA CTCTGCACCC CTGCTTCGGA 540 GCTTTGAAAG GGTGCACAGC ACACCCGCCC TCTCTGGGAA CCCTCGGGAG CTTGAGGTTG 600 CCTGATGAAG GGGCTGATGG GTTGAACGCA AAGGGCCCCT CCACCCACCC TTTTTTCTAT 660 CTCCCCAACC AAGCCCTGGT AACAGGCATT TCCGGTTTCC GGCCGGCTCC CTGGTGCTGG 720 GGTGGGGGTG GGGAGTTGAT TGCTGCCGTC GTGCTTGGCT CTGGGTCCCC TTCTCCCAGA 780 CCCCAGAGGC CTCTGTCCCT GCACACTGCT TCCCCGAAGG AGCGTGGAAA GCCAGCCGAC 840 CTTTCTGGCT CTTTCTTCAT CTTGGGCAGG GGTTTTGTTG ATGGGAGGCT GGCTGGCAAA 900 TGGGGAAGAA TGAACCTCAG GGTTCACCGC AGTGCGCCTG GGTGCTGATT TGCATATGGG 960 CACGATGCCA GCACAGTGGG 980
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