Variant report

Variant rs16881189
Chromosome Location chr5:52552582-52552583
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:52541800-52559200 Weak transcription Breast Myoepithelial Primary Cells Breast
2 chr5:52548200-52554400 Enhancers NHEK skin
3 chr5:52548600-52561400 Enhancers HMEC breast
4 chr5:52549800-52552800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr5:52550000-52552600 Weak transcription HSMMtube muscle
6 chr5:52550000-52558800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
7 chr5:52550200-52552800 Weak transcription Muscle Satellite Cultured Cells --
8 chr5:52550200-52552800 Weak transcription HSMM muscle
9 chr5:52550200-52556600 Weak transcription NHDF-Ad bronchial
10 chr5:52550200-52556800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
11 chr5:52551200-52556400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
12 chr5:52551800-52554800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr5:52552000-52553000 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
14 chr5:52552000-52553600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr5:52552200-52555600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
16 chr5:52552400-52552800 Weak transcription NHLF lung
17 chr5:52552400-52553400 Enhancers NH-A brain
18 chr5:52552400-52554000 Enhancers Osteobl bone

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