Variant report

Variant rs11128839
Chromosome Location chr3:17703391-17703392
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:17668800-17706200 Weak transcription Primary B cells from cord blood blood
2 chr3:17681800-17714400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr3:17689200-17704000 Weak transcription Primary B cells from peripheral blood blood
4 chr3:17694400-17721800 Weak transcription A549 lung
5 chr3:17695000-17706200 Weak transcription Primary hematopoietic stem cells short term culture blood
6 chr3:17697600-17707000 Weak transcription Sigmoid Colon Sigmoid Colon
7 chr3:17697800-17705600 Weak transcription Brain Cingulate Gyrus brain
8 chr3:17697800-17706200 Weak transcription Brain Hippocampus Middle brain
9 chr3:17698000-17706000 Weak transcription Brain Substantia Nigra brain
10 chr3:17698600-17706000 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
11 chr3:17698600-17706600 Weak transcription Left Ventricle heart
12 chr3:17702000-17705800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
13 chr3:17702200-17718400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
14 chr3:17702200-17719000 Weak transcription Dnd41 blood
15 chr3:17702600-17706200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
16 chr3:17703000-17714200 Weak transcription Breast Myoepithelial Primary Cells Breast

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