Variant report
Variant | rs531350652 |
---|---|
Chromosome Location | chr5:35741521-35741522 |
allele | G/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:35737400-35743000 | Weak transcription | Fetal Kidney | kidney |
2 | chr5:35739600-35741600 | Enhancers | Foreskin Fibroblast Primary Cells skin01 | Skin |
3 | chr5:35739800-35742600 | Weak transcription | Pancreas | Pancrea |
4 | chr5:35740400-35742000 | Enhancers | HepG2 | liver |
5 | chr5:35740600-35742000 | Enhancers | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
6 | chr5:35741200-35741600 | Enhancers | Pancreatic Islets | Pancreatic Islet |
7 | chr5:35741200-35742000 | Enhancers | Liver | Liver |
8 | chr5:35741200-35742000 | Enhancers | Hela-S3 | cervix |
9 | chr5:35741200-35742200 | Enhancers | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
10 | chr5:35741200-35742800 | Enhancers | NHDF-Ad | bronchial |
11 | chr5:35741400-35741600 | Flanking Active TSS | Muscle Satellite Cultured Cells | -- |
12 | chr5:35741400-35741600 | Flanking Active TSS | Osteobl | bone |
13 | chr5:35741400-35742000 | Enhancers | HUVEC | blood vessel |