Variant report

Variant rs10895931
Chromosome Location chr11:106064055-106064056
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:6 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:106057400-106071800 Weak transcription Pancreas Pancrea
2 chr11:106063000-106065000 Enhancers Fetal Adrenal Gland Adrenal Gland
3 chr11:106063600-106064200 Enhancers HMEC breast
4 chr11:106063600-106064400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr11:106063800-106065200 Enhancers Fetal Brain Male brain
6 chr11:106064000-106064200 Enhancers Fetal Intestine Large intestine

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