Variant report

Variant rs10817438
Chromosome Location chr9:115874688-115874689
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:115874000-115875000 ZNF genes & repeats HUES48 Cell Line embryonic stem cell
2 chr9:115874000-115875000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr9:115874000-115875000 Enhancers Monocytes-CD14+_RO01746 blood
4 chr9:115874000-115875000 Enhancers NHEK skin
5 chr9:115874000-115875200 Flanking Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr9:115874000-115875200 Enhancers Primary monocytes fromperipheralblood blood
7 chr9:115874000-115875200 Enhancers Primary neutrophils fromperipheralblood blood
8 chr9:115874000-115875200 Flanking Active TSS Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
9 chr9:115874000-115875200 Enhancers Brain Hippocampus Middle brain
10 chr9:115874000-115875200 Enhancers HMEC breast
11 chr9:115874000-115875200 Enhancers HSMM muscle
12 chr9:115874200-115875200 Enhancers Adipose Nuclei Adipose
13 chr9:115874400-115874800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
14 chr9:115874400-115874800 Weak transcription Brain Anterior Caudate brain
15 chr9:115874400-115874800 Weak transcription Brain Inferior Temporal Lobe brain
16 chr9:115874400-115875200 Enhancers Osteobl bone
17 chr9:115874600-115874800 Bivalent Enhancer Primary T killer naive cells fromperipheralblood blood
18 chr9:115874600-115874800 Enhancers Muscle Satellite Cultured Cells --

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