Tag | Content |
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EnhancerAtlas ID | HS184-15502 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr19:38553560-38554400 |
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) |
ZNF263 | MA0528.1 | chr19:38553832-38553853 | TCCCCTCCACCCCCCTCCCCA | - | 6.35 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_10857 | chr19:38548064-38555238 | CD20 | SE_33570 | chr19:38547726-38556155 | H2171 | SE_61973 | chr19:38519548-38571581 | Toledo | SE_63333 | chr19:38548346-38569687 | NCI-H82 | SE_65256 | chr19:38551210-38555782 | Pancreatic_islets | SE_66973 | chr19:38547726-38556155 | H2171 |
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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 |
GH19I038062 | chr19 | 38553425 | 38555011 |
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Enhancer Sequence | GATGTTCTCA AATGGGGTGG CCCCATGAGT TGTCACGAGG GCAGACTCGA GTCAGCCAAT 60 CCCAGGTTCA GATTCCGGCT CCTCCTCCCC TTCTCTTTGT GGCCCTCTCT GAACCCCATT 120 GTGAAGCACG GGTGACAGTA GCAGGTGATT AGAAGCTTCA GTGCAATGGT TTGTGTTATG 180 GTGTCATGTG CTCTGCACAG GGCCTGGCTC CCCGACAGCC CTGGGTCAGG GGCCAGTTAG 240 GATGATGGAT GATTACTGCC AGCAGCTGGG TTTCCCCTCC ACCCCCCTCC CCACTCCAAC 300 CTGGATAACA AGGCCCAGCT GTGTGTGTCC AGCACCTGCA CCGCCCCCGC CGGCCCCCAG 360 CTCCCATCCC TGCCAGCCTT CCCACGGCAG GGAGCCTTCC TGGCTGTGGT GTTCCGGGTG 420 GGCCCCACTG CCGCCCCCCA TCCCCTCAGC CTAGAGCCAT CCTCAGGTTA GGATAAGCAG 480 AGCCGGAGCC ACCCTCAGCC CGGCCCCCAG CGGCAGGATG GAAAGAGTGG GACTTTAACA 540 GATGTTCTTT TACAAGGATT CCCTGGCTCT ATTTAATCAA GATTGTCGAA TATTGATTTA 600 ATCTCCAGGC CCAACAGATG CGGTCTTAGC AGGTTTCAGT GGCAATTAGC TGGGATCAGT 660 TTGCAGGTCA GGCTCCGTGC TGGCAAGACA CTGTCTTCTA AAGGAGGCTT GGCCTGGCCA 720 CAGGAGTGAG CCCTGGAGGA GGGCGCGTAC TAAGTATTTA ACCATCAGTC TAGCCCGGGC 780 AGTGGCCCAC GGGAGCAGGC CCGCAGGCTG GGTCATAGCA GCCCCTGTGG GGCCCCAGTG 840
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