Variant report

Variant rs11884373
Chromosome Location chr2:160926150-160926151
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:3 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:160921000-160930200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr2:160922600-160928000 Weak transcription Fetal Intestine Large intestine
3 chr2:160926000-160926200 ZNF genes & repeats Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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