Variant report

Variant rs7666156
Chromosome Location chr4:100920121-100920122
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:100918600-100920200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
2 chr4:100918800-100920200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr4:100918800-100920200 Enhancers Muscle Satellite Cultured Cells --
4 chr4:100918800-100920200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr4:100918800-100920600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
6 chr4:100919000-100920200 Enhancers Brain Inferior Temporal Lobe brain
7 chr4:100919000-100920200 Enhancers NHEK skin
8 chr4:100919400-100920200 Enhancers Brain Hippocampus Middle brain
9 chr4:100919400-100920200 Enhancers HSMM muscle
10 chr4:100919600-100920200 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
11 chr4:100919600-100920200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr4:100919800-100920200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr4:100919800-100920200 Enhancers HMEC breast
14 chr4:100919800-100920600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin

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