Variant report

Variant rs12238753
Chromosome Location chr9:17251993-17251994
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:17223600-17279400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr9:17236400-17262000 Weak transcription Ovary ovary
3 chr9:17247400-17269000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
4 chr9:17249600-17252000 ZNF genes & repeats Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chr9:17249600-17252400 ZNF genes & repeats Liver Liver
6 chr9:17249600-17252400 ZNF genes & repeats Fetal Lung lung
7 chr9:17249600-17253000 ZNF genes & repeats Monocytes-CD14+_RO01746 blood
8 chr9:17249600-17254600 ZNF genes & repeats Primary hematopoietic stem cells G-CSF-mobilized Male --
9 chr9:17250800-17252600 ZNF genes & repeats Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
10 chr9:17250800-17252600 ZNF genes & repeats Duodenum Smooth Muscle Duodenum
11 chr9:17251000-17252200 ZNF genes & repeats Fetal Kidney kidney
12 chr9:17251800-17252000 ZNF genes & repeats iPS-20b Cell Line embryonic stem cell

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