Variant report

Variant rs41297197
Chromosome Location chr9:116190531-116190532
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:116184600-116199200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr9:116186000-116199200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
3 chr9:116189000-116190800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
4 chr9:116189200-116190600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
5 chr9:116189600-116191000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
6 chr9:116189600-116191200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr9:116189600-116191600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
8 chr9:116190400-116190800 Enhancers Primary hematopoietic stem cells blood
9 chr9:116190400-116191000 Enhancers Primary neutrophils fromperipheralblood blood
10 chr9:116190400-116191000 Genic enhancers Primary hematopoietic stem cells short term culture blood

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