Variant report

Variant rs145280302
Chromosome Location chr6:161845548-161845549
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:161837400-161845600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
2 chr6:161839800-161847000 Weak transcription Pancreatic Islets Pancreatic Islet
3 chr6:161843400-161846000 Enhancers Muscle Satellite Cultured Cells --
4 chr6:161843600-161846400 Enhancers HSMM muscle
5 chr6:161843800-161846000 Enhancers Skeletal Muscle Male skeletal muscle
6 chr6:161843800-161846000 Enhancers HSMMtube muscle
7 chr6:161844000-161845600 Weak transcription NHEK skin
8 chr6:161844200-161845600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
9 chr6:161844600-161845600 Weak transcription Psoas Muscle Psoas
10 chr6:161844600-161845600 Weak transcription Right Ventricle heart
11 chr6:161844800-161845600 Weak transcription Left Ventricle heart
12 chr6:161844800-161845600 Weak transcription NHDF-Ad bronchial
13 chr6:161845400-161846200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr6:161845400-161846400 Enhancers Skeletal Muscle Female skeletal muscle
15 chr6:161845400-161846600 Enhancers HMEC breast

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