Variant report

Variant rs2189670
Chromosome Location chr12:1625937-1625938
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:1612200-1626000 Weak transcription Muscle Satellite Cultured Cells --
2 chr12:1614200-1626200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
3 chr12:1619000-1626000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr12:1619600-1626400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
5 chr12:1621400-1626000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr12:1624200-1626600 Weak transcription HSMM muscle
7 chr12:1625600-1626400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
8 chr12:1625800-1626400 Enhancers NHEK skin

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