Variant report

Variant rs146761539
Chromosome Location chr6:29765123-29765124
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:29761000-29765200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
2 chr6:29761800-29766200 Weak transcription Pancreas Pancrea
3 chr6:29763800-29766000 Enhancers HMEC breast
4 chr6:29763800-29766200 Enhancers NHEK skin
5 chr6:29763800-29766800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr6:29764000-29766000 Enhancers NHDF-Ad bronchial
7 chr6:29764400-29765400 Enhancers Hela-S3 cervix
8 chr6:29764600-29766200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr6:29764800-29780600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr6:29765000-29765400 Bivalent Enhancer Muscle Satellite Cultured Cells --
11 chr6:29765000-29765400 Enhancers Stomach Mucosa stomach

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