Variant report

Variant rs7021688
Chromosome Location chr9:116190841-116190842
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 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 chr9:116189600-116191000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
4 chr9:116189600-116191200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr9:116189600-116191600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
6 chr9:116190400-116191000 Enhancers Primary neutrophils fromperipheralblood blood
7 chr9:116190400-116191000 Genic enhancers Primary hematopoietic stem cells short term culture blood
8 chr9:116190600-116191200 Genic enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
9 chr9:116190800-116191000 Genic enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
10 chr9:116190800-116191000 Enhancers Fetal Stomach stomach
11 chr9:116190800-116191600 Weak transcription Primary hematopoietic stem cells blood

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