Variant report

Variant rs4942851
Chromosome Location chr13:50168965-50168966
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:3 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:50160600-50169200 Weak transcription Esophagus oesophagus
2 chr13:50168400-50169200 Enhancers HepG2 liver
3 chr13:50168800-50169000 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin01 Skin

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