Variant report

Variant rs182753880
Chromosome Location chr9:115823685-115823686
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:115822400-115824000 Weak transcription Right Ventricle heart
2 chr9:115823400-115825400 Bivalent Enhancer Fetal Muscle Trunk muscle
3 chr9:115823400-115825600 ZNF genes & repeats Primary hematopoietic stem cells short term culture blood
4 chr9:115823400-115825600 ZNF genes & repeats Duodenum Mucosa Duodenum
5 chr9:115823400-115825600 ZNF genes & repeats Lung lung
6 chr9:115823400-115825800 ZNF genes & repeats Primary hematopoietic stem cells G-CSF-mobilized Male --
7 chr9:115823600-115823800 Bivalent Enhancer Primary T cells fromperipheralblood blood
8 chr9:115823600-115823800 Bivalent Enhancer Brain Dorsolateral Prefrontal Cortex brain
9 chr9:115823600-115824000 Bivalent Enhancer Fetal Stomach stomach
10 chr9:115823600-115824400 ZNF genes & repeats H1 Derived Mesenchymal Stem Cells ES cell derived
11 chr9:115823600-115824400 Bivalent Enhancer iPS DF 19.11 Cell Line embryonic stem cell
12 chr9:115823600-115824400 Bivalent Enhancer Fetal Brain Male brain
13 chr9:115823600-115825600 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
14 chr9:115823600-115825600 ZNF genes & repeats Primary neutrophils fromperipheralblood blood
15 chr9:115823600-115825600 ZNF genes & repeats Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
16 chr9:115823600-115825600 ZNF genes & repeats Foreskin Melanocyte Primary Cells skin01 Skin

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