Variant report

Variant rs10198425
Chromosome Location chr2:173569393-173569394
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:173564000-173571600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr2:173564200-173575600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr2:173565800-173577200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr2:173566000-173575400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
5 chr2:173568800-173569400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
6 chr2:173569000-173569400 Enhancers Breast Myoepithelial Primary Cells Breast
7 chr2:173569000-173569400 Enhancers Primary T helper naive cells from peripheral blood blood
8 chr2:173569200-173569400 Bivalent Enhancer Primary mononuclear cells fromperipheralblood Blood

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