Variant report

Variant rs73027809
Chromosome Location chr2:168038635-168038636
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:168036400-168039000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
2 chr2:168037200-168038800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
3 chr2:168037200-168039000 Enhancers NHEK skin
4 chr2:168037200-168039200 Enhancers HMEC breast
5 chr2:168037200-168039200 Enhancers NHLF lung
6 chr2:168037400-168038800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr2:168037400-168038800 Enhancers HSMM muscle
8 chr2:168037400-168038800 Enhancers NH-A brain
9 chr2:168037400-168038800 Enhancers Osteobl bone
10 chr2:168037600-168039200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr2:168037800-168039000 Enhancers Muscle Satellite Cultured Cells --
12 chr2:168037800-168043800 Weak transcription Gastric stomach
13 chr2:168038400-168039000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr2:168038600-168038800 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
15 chr2:168038600-168042600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived

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