Variant report

Variant rs1452290
Chromosome Location chr10:48592208-48592209
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:48575600-48598200 Weak transcription NH-A brain
2 chr10:48589600-48592400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
3 chr10:48591400-48592600 Enhancers Fetal Adrenal Gland Adrenal Gland
4 chr10:48591400-48594000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr10:48591600-48592400 Enhancers Osteobl bone
6 chr10:48591600-48593200 Enhancers NHEK skin
7 chr10:48591800-48593000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr10:48591800-48593400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr10:48592000-48593000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr10:48592000-48593000 Enhancers NHDF-Ad bronchial
11 chr10:48592000-48593200 Enhancers HMEC breast
12 chr10:48592000-48593600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr10:48592200-48593000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
14 chr10:48592200-48593200 Enhancers Monocytes-CD14+_RO01746 blood

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