Variant report

Variant rs10854252
Chromosome Location chr20:23669305-23669306
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:6 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:23663800-23672400 Weak transcription NHLF lung
2 chr20:23667000-23672200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr20:23668600-23670000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
4 chr20:23669000-23669800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
5 chr20:23669000-23671000 Enhancers HUVEC blood vessel
6 chr20:23669200-23670200 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin

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