Variant report

Variant rs6885381
Chromosome Location chr5:95617238-95617239
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:95612600-95632400 Weak transcription Aorta Aorta
2 chr5:95613000-95623800 Weak transcription HSMM muscle
3 chr5:95614400-95617400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr5:95614800-95617400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
5 chr5:95614800-95617400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr5:95615600-95617400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr5:95616000-95617400 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
8 chr5:95616000-95618000 Enhancers HMEC breast
9 chr5:95616200-95617600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr5:95616200-95617600 Enhancers NHDF-Ad bronchial
11 chr5:95616400-95617800 Enhancers NHEK skin
12 chr5:95616400-95623000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
13 chr5:95617200-95617800 Enhancers Esophagus oesophagus
14 chr5:95617200-95619400 Weak transcription Pancreatic Islets Pancreatic Islet

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