Variant report

Variant rs1285019
Chromosome Location chr6:45167672-45167673
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:45162000-45171800 Enhancers Dnd41 blood
2 chr6:45166400-45167800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
3 chr6:45167000-45167800 Enhancers Fetal Intestine Small intestine
4 chr6:45167000-45168200 Enhancers Fetal Intestine Large intestine
5 chr6:45167000-45168800 Enhancers Liver Liver
6 chr6:45167200-45167800 Enhancers Primary T cells from cord blood blood
7 chr6:45167200-45167800 Enhancers Primary T killer naive cells fromperipheralblood blood
8 chr6:45167200-45168400 Flanking Active TSS HepG2 liver
9 chr6:45167200-45168600 Enhancers Pancreatic Islets Pancreatic Islet
10 chr6:45167400-45167800 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr6:45167400-45167800 Enhancers Fetal Lung lung

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