Variant report

Variant rs191966986
Chromosome Location chr7:16358907-16358908
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 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 chr7:16358200-16359400 Enhancers HMEC breast
5 chr7:16358200-16359400 Enhancers NHEK skin
6 chr7:16358200-16359600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
7 chr7:16358200-16359600 Enhancers HUVEC blood vessel
8 chr7:16358200-16359600 Enhancers Osteobl bone
9 chr7:16358200-16359800 Enhancers NH-A brain
10 chr7:16358400-16359200 Enhancers A549 lung
11 chr7:16358400-16359400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr7:16358400-16359400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr7:16358400-16359600 Enhancers Muscle Satellite Cultured Cells --
14 chr7:16358400-16359600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
15 chr7:16358600-16359000 Weak transcription Gastric stomach
16 chr7:16358600-16359200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
17 chr7:16358800-16359200 Enhancers HSMM muscle
18 chr7:16358800-16359400 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin

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