Variant report

Variant rs534791800
Chromosome Location chr6:161845784-161845785
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:161839800-161847000 Weak transcription Pancreatic Islets Pancreatic Islet
2 chr6:161843400-161846000 Enhancers Muscle Satellite Cultured Cells --
3 chr6:161843600-161846400 Enhancers HSMM muscle
4 chr6:161843800-161846000 Enhancers Skeletal Muscle Male skeletal muscle
5 chr6:161843800-161846000 Enhancers HSMMtube muscle
6 chr6:161845400-161846200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr6:161845400-161846400 Enhancers Skeletal Muscle Female skeletal muscle
8 chr6:161845400-161846600 Enhancers HMEC breast
9 chr6:161845600-161845800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
10 chr6:161845600-161845800 Enhancers Left Ventricle heart
11 chr6:161845600-161845800 Enhancers Psoas Muscle Psoas
12 chr6:161845600-161845800 Enhancers Right Ventricle heart
13 chr6:161845600-161845800 Enhancers NHDF-Ad bronchial
14 chr6:161845600-161846000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr6:161845600-161846000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
16 chr6:161845600-161846000 Enhancers NHEK skin

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