Variant report

Variant rs61892575
Chromosome Location chr11:10225574-10225575
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 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 chr11:10215000-10226200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr11:10219000-10242200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr11:10219800-10226400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
6 chr11:10221600-10227000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
7 chr11:10223400-10226400 Weak transcription Left Ventricle heart
8 chr11:10223800-10229600 Weak transcription Osteobl bone
9 chr11:10224400-10226000 ZNF genes & repeats Monocytes-CD14+_RO01746 blood
10 chr11:10224600-10226600 ZNF genes & repeats iPS-20b Cell Line embryonic stem cell
11 chr11:10224800-10225600 ZNF genes & repeats Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
12 chr11:10224800-10226000 ZNF genes & repeats Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr11:10224800-10227200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
14 chr11:10225000-10226800 Weak transcription iPS-15b Cell Line embryonic stem cell
15 chr11:10225000-10227000 Weak transcription H1 Cell Line embryonic stem cell
16 chr11:10225400-10227400 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived

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