Variant report

Variant rs145564139
Chromosome Location chr11:66226790-66226791
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:66219800-66233800 Weak transcription Aorta Aorta
2 chr11:66223600-66227600 Enhancers Primary B cells from cord blood blood
3 chr11:66223600-66227600 Enhancers Primary B cells from peripheral blood blood
4 chr11:66223800-66232400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr11:66224200-66226800 Weak transcription Stomach Smooth Muscle stomach
6 chr11:66224800-66227600 Enhancers Primary monocytes fromperipheralblood blood
7 chr11:66226200-66227000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
8 chr11:66226200-66227000 Enhancers Primary hematopoietic stem cells short term culture blood
9 chr11:66226200-66227000 Flanking Active TSS Monocytes-CD14+_RO01746 blood
10 chr11:66226200-66227200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr11:66226400-66227000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
12 chr11:66226400-66227400 Enhancers Primary Natural Killer cells fromperipheralblood blood
13 chr11:66226400-66227400 Enhancers Primary mononuclear cells fromperipheralblood Blood
14 chr11:66226600-66226800 Enhancers Placenta Amnion Placenta Amnion
15 chr11:66226600-66227000 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
16 chr11:66226600-66227000 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin01 Skin
17 chr11:66226600-66227000 Enhancers K562 blood
18 chr11:66226600-66227400 Flanking Active TSS GM12878-XiMat blood

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