Tag | Content |
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EnhancerAtlas ID | HS193-16359 |
Organism | Homo sapiens |
Tissue/cell | U87 |
Coordinate | chr19:19701620-19702810 |
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) |
JUN(var.2) | MA0489.1 | chr19:19702034-19702048 | GAGAGGTGACTCAT | + | 6.35 | LMX1B | MA0703.2 | chr19:19701796-19701807 | GTTTTAATTAA | + | 6.14 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_12109 | chr19:19700241-19703035 | CD3 | SE_18839 | chr19:19700276-19704898 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19648 | chr19:19700122-19703992 | CD4p_CD25-_Il17p_PMAstim_Th17 |
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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 |
GH19I019589 | chr19 | 19700502 | 19703700 |
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Enhancer Sequence | CAGATTCCTT AATCTGTATA TTTATATACA ATGATCCACT TCTCTGTCCA ACAGACACTT 60 TGGCAATGAT AGGATGTTCT AGACCTTTCT ATTATAGGAG GCACCAGCCC TGTGTGGCTG 120 CTGAGACTTG AAATGTGGCT GGTGTGGCTG AGGAATGCAC TGGTTAATTG CATTTGGTTT 180 TAATTAATTC AAATGTAAAC AGCCCTGCGT TGAGTATCTG GAGCCACCCA GCTGATGAGA 240 CTCAGGGGCT CAATTTGTGA GTTACCCTGA GACTGAGGGG AGGAAAGGAT ACTCCAATCA 300 ACCTGGAGAA TAAGTCCCCC AGCTGCCGGG GTCTACTCCC ACAAGAACCC TAAAGAAATG 360 TACATGGGAC TCAGCCCCAG GGTACAGCTA ATTAGAAAAA GGATCTCAGT TCCAGAGAGG 420 TGACTCATAG GCCTCAGGGT GACTGCTAGG ACCCAGGAAA GCCCCATGAG CACCATGACA 480 CCCCAGCTTC CTGGCTGAAT TTACAGAACC CGATTCTGTA ATTGCAACAG ATCCGACCAG 540 CTGACGAGGA AGGGAAAGAA TGAGAATGGC TTATGCCTGC CAACTACTAG CAAGGCCAAT 600 CATTAGTCAG GAAGACAAAA AGGCATTCCC TGATGTTATG CATTATTTAC ATTTACTCCT 660 CTGAATGGGG CTCTGTGCGT TCCTACAGCA CAGCAAGGGT TCCTGCAGCA CAACAGCCCT 720 GGCTGAGAAA CTTCTTGTTC CCCAGAGACA CAGTCACAGG GTGGAGAAGG CAAAGCAGGC 780 CCCTTCTCAA GAACGGCCCA GGATGGGATG GCCGAGTGGG TCTGCAAGGG GCCTCTGGGG 840 CTCAGCACAC CGCCTCGGAG CTGCCTACCC ACTCGAGATC TGAGATCCGA AGCTTTTCAC 900 ACAAGCTGTC ACTCATGCTC ATGTGGAGGT AAAGCCTGAC ACATTCCAAC GTGCCAGGCT 960 GTCCCTGCTC TGGTGCCAAA CACCACTGTG TGAATTCAGG CCACGCCTCA GTCCTCACTG 1020 GGAACATCAA TGTGACAAAC CTTATTTTTT ATTTTTATAT TTTTTTAGAG GCAGAGTCTC 1080 ACTTTGTCGC CCAAGCTGGG GTGCAGTGGT GTGATCTCAG CTCACTGCAA ACCTCACATC 1140 CCAGGTTCAA GTGATTCTTC TGCCTCAGCC TCCCGTGTAG CTAGGATTAT 1190
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