Tag | Content |
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EnhancerAtlas ID | HS060-17595 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr19:19701790-19702610 |
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 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH19I019589 | chr19 | 19700502 | 19703700 |
|
Enhancer Sequence | CATTTGGTTT TAATTAATTC AAATGTAAAC AGCCCTGCGT TGAGTATCTG GAGCCACCCA 60 GCTGATGAGA CTCAGGGGCT CAATTTGTGA GTTACCCTGA GACTGAGGGG AGGAAAGGAT 120 ACTCCAATCA ACCTGGAGAA TAAGTCCCCC AGCTGCCGGG GTCTACTCCC ACAAGAACCC 180 TAAAGAAATG TACATGGGAC TCAGCCCCAG GGTACAGCTA ATTAGAAAAA GGATCTCAGT 240 TCCAGAGAGG TGACTCATAG GCCTCAGGGT GACTGCTAGG ACCCAGGAAA GCCCCATGAG 300 CACCATGACA CCCCAGCTTC CTGGCTGAAT TTACAGAACC CGATTCTGTA ATTGCAACAG 360 ATCCGACCAG CTGACGAGGA AGGGAAAGAA TGAGAATGGC TTATGCCTGC CAACTACTAG 420 CAAGGCCAAT CATTAGTCAG GAAGACAAAA AGGCATTCCC TGATGTTATG CATTATTTAC 480 ATTTACTCCT CTGAATGGGG CTCTGTGCGT TCCTACAGCA CAGCAAGGGT TCCTGCAGCA 540 CAACAGCCCT GGCTGAGAAA CTTCTTGTTC CCCAGAGACA CAGTCACAGG GTGGAGAAGG 600 CAAAGCAGGC CCCTTCTCAA GAACGGCCCA GGATGGGATG GCCGAGTGGG TCTGCAAGGG 660 GCCTCTGGGG CTCAGCACAC CGCCTCGGAG CTGCCTACCC ACTCGAGATC TGAGATCCGA 720 AGCTTTTCAC ACAAGCTGTC ACTCATGCTC ATGTGGAGGT AAAGCCTGAC ACATTCCAAC 780 GTGCCAGGCT GTCCCTGCTC TGGTGCCAAA CACCACTGTG 820
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