Variant report

Variant rs115528611
Chromosome Location chr11:10226983-10226984
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:10208000-10229000 Weak transcription Aorta Aorta
2 chr11:10208800-10229400 Weak transcription NHLF lung
3 chr11:10219000-10242200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr11:10221600-10227000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
5 chr11:10223800-10229600 Weak transcription Osteobl bone
6 chr11:10224800-10227200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
7 chr11:10225000-10227000 Weak transcription H1 Cell Line embryonic stem cell
8 chr11:10225400-10227400 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
9 chr11:10225600-10228400 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
10 chr11:10226000-10227400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr11:10226200-10227000 ZNF genes & repeats hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
12 chr11:10226200-10227400 ZNF genes & repeats Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr11:10226400-10227400 ZNF genes & repeats Foreskin Fibroblast Primary Cells skin01 Skin
14 chr11:10226400-10227800 Enhancers Left Ventricle heart
15 chr11:10226800-10227000 Weak transcription Ovary ovary
16 chr11:10226800-10227200 Enhancers iPS-20b Cell Line embryonic stem cell
17 chr11:10226800-10227600 Enhancers HUES48 Cell Line embryonic stem cell
18 chr11:10226800-10230000 Enhancers iPS-15b Cell Line embryonic stem cell

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