Variant report

Variant rs17308929
Chromosome Location chr11:26256244-26256245
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:26251800-26259200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
2 chr11:26255600-26256800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr11:26255800-26256600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
4 chr11:26255800-26256800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr11:26255800-26256800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr11:26255800-26256800 Enhancers HUVEC blood vessel
7 chr11:26255800-26256800 Enhancers NHEK skin
8 chr11:26256000-26256600 Enhancers Muscle Satellite Cultured Cells --
9 chr11:26256000-26256800 Enhancers Hela-S3 cervix
10 chr11:26256200-26256400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
11 chr11:26256200-26256600 Enhancers HMEC breast

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