Variant report

Variant rs532834235
Chromosome Location chr16:12704447-12704448
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr16:12703400-12706400 Enhancers HepG2 liver
2 chr16:12703400-12706800 Enhancers Liver Liver
3 chr16:12703600-12704600 Enhancers Cortex derived primary cultured neurospheres brain
4 chr16:12703800-12704600 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
5 chr16:12703800-12706800 Enhancers K562 blood
6 chr16:12703800-12708000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr16:12704000-12708800 Enhancers Placenta Placenta
8 chr16:12704200-12708400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
9 chr16:12704400-12705600 Enhancers A549 lung
10 chr16:12704400-12707400 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
11 chr16:12704400-12707400 Enhancers Stomach Mucosa stomach

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