Variant report
Variant | rs16945816 |
---|---|
Chromosome Location | chr16:48151198-48151199 |
allele | A/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr16:48146400-48160600 | Weak transcription | Right Atrium | heart |
2 | chr16:48147400-48151400 | Weak transcription | Pancreas | Pancrea |
3 | chr16:48147600-48160600 | Weak transcription | Psoas Muscle | Psoas |
4 | chr16:48149600-48151200 | Weak transcription | Right Ventricle | heart |
5 | chr16:48150600-48151400 | Enhancers | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
6 | chr16:48151000-48151200 | Bivalent Enhancer | Primary T cells fromperipheralblood | blood |
7 | chr16:48151000-48151200 | Bivalent Enhancer | Foreskin Fibroblast Primary Cells skin01 | Skin |
8 | chr16:48151000-48151200 | Bivalent Enhancer | HepG2 | liver |
9 | chr16:48151000-48152200 | Enhancers | iPS DF 19.11 Cell Line | embryonic stem cell |
10 | chr16:48151000-48152800 | Enhancers | A549 | lung |
11 | chr16:48151000-48153200 | Enhancers | Fetal Adrenal Gland | Adrenal Gland |