Variant report

Variant rs532919875
Chromosome Location chr14:21423587-21423588
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:21420200-21423600 Enhancers Primary hematopoietic stem cells short term culture blood
2 chr14:21422400-21424000 Enhancers Liver Liver
3 chr14:21422400-21425400 Enhancers Fetal Thymus thymus
4 chr14:21422600-21424400 Enhancers HepG2 liver
5 chr14:21423000-21423600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
6 chr14:21423000-21424600 Active TSS Brain Hippocampus Middle brain
7 chr14:21423000-21424600 Flanking Active TSS Monocytes-CD14+_RO01746 blood
8 chr14:21423200-21423800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr14:21423200-21423800 Flanking Active TSS Primary neutrophils fromperipheralblood blood
10 chr14:21423200-21423800 Enhancers Adipose Nuclei Adipose
11 chr14:21423200-21424000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
12 chr14:21423200-21424200 Flanking Active TSS Primary monocytes fromperipheralblood blood
13 chr14:21423200-21424200 Enhancers Primary hematopoietic stem cells blood
14 chr14:21423200-21424200 Enhancers Thymus Thymus
15 chr14:21423400-21424400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --

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