Variant report

Variant rs17735908
Chromosome Location chr1:214748651-214748652
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:214747000-214748800 Enhancers Breast Myoepithelial Primary Cells Breast
2 chr1:214747000-214748800 Enhancers Hela-S3 cervix
3 chr1:214747800-214749400 Weak transcription Colon Smooth Muscle Colon
4 chr1:214748000-214748800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr1:214748000-214749200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr1:214748200-214749400 Enhancers HMEC breast
7 chr1:214748400-214748800 Enhancers Placenta Placenta
8 chr1:214748600-214749200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
9 chr1:214748600-214749200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr1:214748600-214749200 Enhancers NHEK skin
11 chr1:214748600-214754800 Weak transcription Skeletal Muscle Female skeletal muscle

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