Variant report

Variant rs1448664
Chromosome Location chr7:17641577-17641578
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:17638000-17641600 Enhancers Stomach Mucosa stomach
2 chr7:17638000-17642000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr7:17638000-17642200 Enhancers HMEC breast
4 chr7:17638000-17643000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr7:17638400-17641800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
6 chr7:17638400-17642200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr7:17638400-17642200 Enhancers NHDF-Ad bronchial
8 chr7:17639800-17642800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr7:17640000-17642600 Enhancers Hela-S3 cervix
10 chr7:17640400-17642600 Enhancers NHEK skin
11 chr7:17641400-17641600 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
12 chr7:17641400-17643000 Enhancers Placenta Placenta

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