Tag | Content |
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EnhancerAtlas ID | HS098-26969 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr19:6801070-6802030 |
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 |
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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 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH19I006799 | chr19 | 6799599 | 6804367 |
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Enhancer Sequence | TCATCAATTA TTCACCTTGC TGACTGCTTA GTGTTTGTCT CCTGGCTGGA TTACATAAGC 60 CCTGTAAGGG CAGAGCTCTG TTTGTCTTGA TCACCATTAG GTTCTGGTGC TTGGCATACA 120 GTAGGCATTC CACACATGCT TGCTGAATTA ATGCATGACC GGGTCTGGGG TGCTGGGTTT 180 CACACCAGGC TCTACCGCAA ACATTGGGTC AAGTATTTTC ATTCCCGACG TACAGATGAG 240 TCAATTGAAT CAACGGAAAG CAAAATGATC CCATCCAAGC TCCCTCAACT TGCCGGGCTG 300 GTCTGGGAGT CGAACCAGAT CTGCCTGACC CTCCCACCGG TGCTGAAAAG TGGAGTGTGT 360 GCTGGGGTGG TAGGGGATGG GGCAGAAGAG AGACGGGCTT CCTCACAGAA GGGTTTGAGG 420 GCTAGGATGA GGCGTGCACA CTCTGCACCC CTGCTTCGGA GCTTTGAAAG GGTGCACAGC 480 ACACCCGCCC TCTCTGGGAA CCCTCGGGAG CTTGAGGTTG CCTGATGAAG GGGCTGATGG 540 GTTGAACGCA AAGGGCCCCT CCACCCACCC TTTTTTCTAT CTCCCCAACC AAGCCCTGGT 600 AACAGGCATT TCCGGTTTCC GGCCGGCTCC CTGGTGCTGG GGTGGGGGTG GGGAGTTGAT 660 TGCTGCCGTC GTGCTTGGCT CTGGGTCCCC TTCTCCCAGA CCCCAGAGGC CTCTGTCCCT 720 GCACACTGCT TCCCCGAAGG AGCGTGGAAA GCCAGCCGAC CTTTCTGGCT CTTTCTTCAT 780 CTTGGGCAGG GGTTTTGTTG ATGGGAGGCT GGCTGGCAAA TGGGGAAGAA TGAACCTCAG 840 GGTTCACCGC AGTGCGCCTG GGTGCTGATT TGCATATGGG CACGATGCCA GCACAGTGGG 900 TGCCCGCCTC TTCCTGGAGG AAGGAAGAGG GGCACTGAGG GGGGTTGCCC CCAGCAGGGA 960
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