Variant report

Variant rs9595666
Chromosome Location chr13:47995149-47995150
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:47993200-47995600 Enhancers Fetal Adrenal Gland Adrenal Gland
2 chr13:47993200-47996400 Enhancers NHDF-Ad bronchial
3 chr13:47993400-47995200 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
4 chr13:47993400-47997000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr13:47994000-47995200 Enhancers NHLF lung
6 chr13:47994200-47995800 Enhancers Liver Liver
7 chr13:47994200-47996400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
8 chr13:47994800-47995800 Enhancers Adipose Nuclei Adipose
9 chr13:47995000-47995200 Flanking Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr13:47995000-47995600 Weak transcription Breast Myoepithelial Primary Cells Breast
11 chr13:47995000-48000200 Weak transcription Muscle Satellite Cultured Cells --
12 chr13:47995000-48000400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin

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