Variant report

Variant rs144917291
Chromosome Location chr7:16358481-16358482
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:16357200-16360400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr7:16357200-16372600 Weak transcription K562 blood
3 chr7:16357800-16359800 Enhancers Stomach Mucosa stomach
4 chr7:16358200-16358600 Enhancers Gastric stomach
5 chr7:16358200-16359400 Enhancers HMEC breast
6 chr7:16358200-16359400 Enhancers NHEK skin
7 chr7:16358200-16359600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
8 chr7:16358200-16359600 Enhancers HUVEC blood vessel
9 chr7:16358200-16359600 Enhancers Osteobl bone
10 chr7:16358200-16359800 Enhancers NH-A brain
11 chr7:16358400-16359200 Enhancers A549 lung
12 chr7:16358400-16359400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr7:16358400-16359400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
14 chr7:16358400-16359600 Enhancers Muscle Satellite Cultured Cells --
15 chr7:16358400-16359600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin

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