Variant report

Variant rs138537002
Chromosome Location chr20:14978895-14978896
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:14977200-14979000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
2 chr20:14977200-14979000 Enhancers HMEC breast
3 chr20:14977400-14979000 Genic enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr20:14977400-14979000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr20:14977600-14979000 Enhancers Hela-S3 cervix
6 chr20:14978200-14979000 Enhancers HUVEC blood vessel
7 chr20:14978400-14979000 Enhancers Muscle Satellite Cultured Cells --
8 chr20:14978400-14979000 Enhancers NHEK skin
9 chr20:14978600-14981000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived

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