Variant report

Variant rs10465046
Chromosome Location chr9:17226889-17226890
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:17204600-17236000 Weak transcription Ovary ovary
2 chr9:17207800-17246400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
3 chr9:17217600-17247000 Weak transcription Left Ventricle heart
4 chr9:17220000-17230000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
5 chr9:17222200-17242000 Weak transcription Primary hematopoietic stem cells blood
6 chr9:17223200-17242200 Weak transcription Monocytes-CD14+_RO01746 blood
7 chr9:17223600-17279400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr9:17224200-17227000 Weak transcription Aorta Aorta
9 chr9:17224400-17242800 Weak transcription Colon Smooth Muscle Colon
10 chr9:17224600-17242200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr9:17225200-17242000 Weak transcription Fetal Lung lung
12 chr9:17225400-17230000 Weak transcription Liver Liver
13 chr9:17225400-17246600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
14 chr9:17225600-17228400 Weak transcription Adipose Nuclei Adipose
15 chr9:17225800-17228000 Weak transcription HUVEC blood vessel
16 chr9:17226200-17241000 Weak transcription Breast Myoepithelial Primary Cells Breast
17 chr9:17226400-17230000 Weak transcription Thymus Thymus
18 chr9:17226600-17227200 ZNF genes & repeats Primary hematopoietic stem cells G-CSF-mobilized Male --
19 chr9:17226600-17228200 Strong transcription Primary monocytes fromperipheralblood blood

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