Variant report

Variant rs186595337
Chromosome Location chr4:69360660-69360661
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:69355400-69362000 Weak transcription Esophagus oesophagus
2 chr4:69359400-69360800 Enhancers Primary monocytes fromperipheralblood blood
3 chr4:69359800-69360800 Enhancers Primary hematopoietic stem cells short term culture blood
4 chr4:69360000-69360800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
5 chr4:69360000-69360800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
6 chr4:69360200-69360800 Enhancers Primary B cells from peripheral blood blood
7 chr4:69360200-69360800 Enhancers Primary hematopoietic stem cells blood
8 chr4:69360200-69360800 Enhancers Primary T helper cells fromperipheralblood blood
9 chr4:69360400-69360800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
10 chr4:69360400-69360800 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
11 chr4:69360400-69360800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
12 chr4:69360400-69361000 Enhancers Primary T cells from cord blood blood

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