Variant report

Variant rs72693705
Chromosome Location chr9:21295099-21295100
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:21293600-21295200 Enhancers HMEC breast
2 chr9:21293800-21295400 Enhancers Hela-S3 cervix
3 chr9:21294000-21295400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr9:21294200-21295200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr9:21294400-21295200 Flanking Active TSS GM12878-XiMat blood
6 chr9:21294400-21295400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
7 chr9:21294400-21296800 Enhancers Primary hematopoietic stem cells short term culture blood
8 chr9:21294400-21297000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
9 chr9:21294600-21295600 Bivalent Enhancer Primary B cells from cord blood blood
10 chr9:21294800-21296600 Enhancers Primary hematopoietic stem cells blood
11 chr9:21294800-21296600 Enhancers Monocytes-CD14+_RO01746 blood
12 chr9:21294800-21296800 Enhancers Primary monocytes fromperipheralblood blood
13 chr9:21294800-21296800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
14 chr9:21295000-21296400 Enhancers Primary neutrophils fromperipheralblood blood

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