The 2.0 version of rSNPBase

Variant report

Variant rs16933738
Chromosome Location chr9:15889533-15889534
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:15877000-15903400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr9:15884200-15891800 Weak transcription Breast Myoepithelial Primary Cells Breast
3 chr9:15884200-15892200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
4 chr9:15885800-15892200 Weak transcription Primary hematopoietic stem cells blood
5 chr9:15889000-15890200 Enhancers Placenta Amnion Placenta Amnion
6 chr9:15889000-15890800 Strong transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
7 chr9:15889000-15892800 Strong transcription Foreskin Melanocyte Primary Cells skin03 Skin
8 chr9:15889400-15890200 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
9 chr9:15889400-15890400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived

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Last update: Aug 31, 2015