Variant report

Variant rs569838588
Chromosome Location chr1:241586515-241586516
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:241574200-241587000 Weak transcription Gastric stomach
2 chr1:241577600-241586600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr1:241582200-241586600 Enhancers NHDF-Ad bronchial
4 chr1:241584000-241587000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
5 chr1:241585000-241586600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
6 chr1:241585400-241586800 Enhancers NHLF lung
7 chr1:241585800-241586600 Weak transcription Osteobl bone
8 chr1:241586000-241586600 Enhancers Muscle Satellite Cultured Cells --
9 chr1:241586000-241586800 Active TSS Brain Anterior Caudate brain
10 chr1:241586000-241587000 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin03 Skin
11 chr1:241586200-241586800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
12 chr1:241586400-241586600 Enhancers Fetal Brain Male brain
13 chr1:241586400-241586800 Flanking Active TSS Pancreatic Islets Pancreatic Islet

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