Variant report

Variant rs11706586
Chromosome Location chr3:133394930-133394931
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:133393200-133395800 Enhancers GM12878-XiMat blood
2 chr3:133393600-133395000 Enhancers Liver Liver
3 chr3:133393600-133395200 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland
4 chr3:133393800-133395400 Weak transcription Brain Hippocampus Middle brain
5 chr3:133393800-133395800 Enhancers Adipose Nuclei Adipose
6 chr3:133393800-133396200 Weak transcription Right Atrium heart
7 chr3:133393800-133406800 Weak transcription Brain Substantia Nigra brain
8 chr3:133394000-133395400 Bivalent Enhancer iPS-20b Cell Line embryonic stem cell
9 chr3:133394000-133399600 Weak transcription Brain Inferior Temporal Lobe brain
10 chr3:133394200-133395600 Bivalent Enhancer H9 Derived Neuron Cultured Cells ES cell derived
11 chr3:133394200-133395600 Enhancers Pancreas Pancrea
12 chr3:133394600-133395200 Enhancers H9 Cell Line embryonic stem cell
13 chr3:133394600-133395400 Bivalent Enhancer Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
14 chr3:133394600-133395800 Bivalent Enhancer H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
15 chr3:133394600-133395800 Flanking Active TSS HepG2 liver
16 chr3:133394800-133395400 Bivalent Enhancer Fetal Intestine Large intestine

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