Variant report

Variant rs3894436
Chromosome Location chr8:119306274-119306275
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:119299000-119307000 Weak transcription Primary monocytes fromperipheralblood blood
2 chr8:119304200-119322200 Weak transcription GM12878-XiMat blood
3 chr8:119305400-119306400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr8:119305400-119306400 Enhancers NHLF lung
5 chr8:119305800-119306800 Bivalent Enhancer IMR90 fetal lung fibroblasts Cell Line lung
6 chr8:119306000-119306600 Enhancers Brain Inferior Temporal Lobe brain
7 chr8:119306000-119306800 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr8:119306000-119306800 Enhancers Brain Hippocampus Middle brain
9 chr8:119306000-119306800 Enhancers Ovary ovary
10 chr8:119306000-119306800 Enhancers Right Atrium heart
11 chr8:119306200-119306400 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
12 chr8:119306200-119306400 Bivalent Enhancer HSMM muscle
13 chr8:119306200-119306400 Bivalent Enhancer NHDF-Ad bronchial
14 chr8:119306200-119306600 Enhancers Cortex derived primary cultured neurospheres brain
15 chr8:119306200-119306600 Enhancers Left Ventricle heart
16 chr8:119306200-119306800 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
17 chr8:119306200-119306800 Enhancers Brain Angular Gyrus brain
18 chr8:119306200-119306800 Enhancers Brain Cingulate Gyrus brain

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