Variant report

Variant rs9364932
Chromosome Location chr6:167809278-167809279
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:5 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:167807400-167809600 Bivalent Enhancer HepG2 liver
2 chr6:167807600-167814400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr6:167809000-167809800 Enhancers Fetal Lung lung
4 chr6:167809200-167812600 Enhancers Liver Liver
5 chr6:167809200-167812800 Enhancers Fetal Intestine Small intestine

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