Variant report

Variant rs150403972
Chromosome Location chr6:29765257-29765258
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:29761800-29766200 Weak transcription Pancreas Pancrea
2 chr6:29763800-29766000 Enhancers HMEC breast
3 chr6:29763800-29766200 Enhancers NHEK skin
4 chr6:29763800-29766800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr6:29764000-29766000 Enhancers NHDF-Ad bronchial
6 chr6:29764400-29765400 Enhancers Hela-S3 cervix
7 chr6:29764600-29766200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr6:29764800-29780600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr6:29765000-29765400 Bivalent Enhancer Muscle Satellite Cultured Cells --
10 chr6:29765000-29765400 Enhancers Stomach Mucosa stomach
11 chr6:29765200-29765600 Enhancers NH-A brain
12 chr6:29765200-29765800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

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