Variant report

Variant rs16853163
Chromosome Location chr2:168039035-168039036
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:168037200-168039200 Enhancers HMEC breast
2 chr2:168037200-168039200 Enhancers NHLF lung
3 chr2:168037600-168039200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr2:168037800-168043800 Weak transcription Gastric stomach
5 chr2:168038600-168042600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
6 chr2:168038800-168046200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
7 chr2:168039000-168040200 Weak transcription Muscle Satellite Cultured Cells --
8 chr2:168039000-168043800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr2:168039000-168048000 Weak transcription NHEK skin
10 chr2:168039000-168053000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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