Variant report

Variant rs572052208
Chromosome Location chr11:93639054-93639055
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:93636400-93639600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
2 chr11:93637400-93641800 Weak transcription HUES6 Cell Line embryonic stem cell
3 chr11:93638200-93639200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr11:93638400-93639200 Enhancers Placenta Placenta
5 chr11:93638400-93639200 Enhancers HSMM muscle
6 chr11:93638400-93640200 Enhancers NH-A brain
7 chr11:93638400-93640400 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
8 chr11:93638400-93640600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr11:93638400-93643000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
10 chr11:93638600-93639200 Enhancers HSMMtube muscle
11 chr11:93638600-93640200 Enhancers NHDF-Ad bronchial
12 chr11:93638600-93642600 Enhancers HMEC breast
13 chr11:93638800-93639600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
14 chr11:93639000-93641200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
15 chr11:93639000-93641200 Weak transcription NHEK skin
16 chr11:93639000-93641400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
17 chr11:93639000-93641400 Weak transcription Osteobl bone

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