Variant report

Variant rs3850959
Chromosome Location chr12:30767141-30767142
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
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

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