Variant report
Variant | rs3850959 |
---|---|
Chromosome Location | chr12:30767141-30767142 |
allele | C/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:30765600-30767600 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
2 | chr12:30765800-30767200 | Enhancers | HepG2 | liver |
3 | chr12:30766000-30767600 | Enhancers | Breast Myoepithelial Primary Cells | Breast |
4 | chr12:30766000-30767600 | Enhancers | Placenta | Placenta |
5 | chr12:30766200-30767200 | Enhancers | Cortex derived primary cultured neurospheres | brain |
6 | chr12:30766400-30767200 | Enhancers | Thymus | Thymus |
7 | chr12:30766600-30767400 | Enhancers | Ganglion Eminence derived primary cultured neurospheres | brain |
8 | chr12:30766800-30770200 | Weak transcription | Liver | Liver |
9 | chr12:30767000-30780800 | Weak transcription | Fetal Muscle Leg | muscle |
10 | chr12:30767000-30784800 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
11 | chr12:30767000-30785600 | Weak transcription | Pancreas | Pancrea |
12 | chr12:30767000-30844200 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |