Variant report

Variant rs566446737
Chromosome Location chr12:1626307-1626308
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:1619600-1626400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
2 chr12:1624200-1626600 Weak transcription HSMM muscle
3 chr12:1625600-1626400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
4 chr12:1625800-1626400 Enhancers NHEK skin
5 chr12:1626000-1626400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr12:1626000-1626400 Enhancers HMEC breast
7 chr12:1626000-1626600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr12:1626000-1627400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr12:1626000-1628000 Enhancers Muscle Satellite Cultured Cells --
10 chr12:1626000-1629400 Enhancers NHDF-Ad bronchial
11 chr12:1626200-1626400 Enhancers Ovary ovary
12 chr12:1626200-1626400 Enhancers Osteobl bone
13 chr12:1626200-1627200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
14 chr12:1626200-1627200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
15 chr12:1626200-1627800 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin

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