Variant report

Variant rs526672
Chromosome Location chr11:59496692-59496693
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:59495000-59496800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
2 chr11:59495200-59499000 Enhancers Primary monocytes fromperipheralblood blood
3 chr11:59495600-59497000 Enhancers Primary hematopoietic stem cells short term culture blood
4 chr11:59495800-59496800 Enhancers K562 blood
5 chr11:59495800-59497400 Enhancers Primary hematopoietic stem cells blood
6 chr11:59496000-59496800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr11:59496000-59496800 Flanking Active TSS Monocytes-CD14+_RO01746 blood
8 chr11:59496000-59497000 Enhancers Primary Natural Killer cells fromperipheralblood blood
9 chr11:59496200-59496800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr11:59496200-59496800 Enhancers NHEK skin
11 chr11:59496200-59497000 Enhancers HUVEC blood vessel
12 chr11:59496400-59496800 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
13 chr11:59496400-59496800 Flanking Active TSS Primary neutrophils fromperipheralblood blood
14 chr11:59496400-59496800 Enhancers Primary T cells fromperipheralblood blood
15 chr11:59496400-59496800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
16 chr11:59496400-59496800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
17 chr11:59496400-59496800 Enhancers HMEC breast

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