Variant report

Variant rs74139652
Chromosome Location chr1:220600821-220600822
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:220598800-220603400 Weak transcription ES-I3 Cell Line embryonic stem cell
2 chr1:220599000-220601400 Enhancers Hela-S3 cervix
3 chr1:220599800-220601000 Enhancers Adipose Nuclei Adipose
4 chr1:220599800-220603200 Weak transcription Placenta Placenta
5 chr1:220600200-220601000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr1:220600200-220601000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr1:220600200-220601000 Enhancers HMEC breast
8 chr1:220600200-220601200 Enhancers NHEK skin
9 chr1:220600600-220601400 Enhancers Pancreatic Islets Pancreatic Islet
10 chr1:220600800-220603200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr1:220600800-220603400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin

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