Variant report

Variant rs188356495
Chromosome Location chr3:69881197-69881198
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:69870200-69886000 Weak transcription Aorta Aorta
2 chr3:69870600-69886200 Weak transcription Colon Smooth Muscle Colon
3 chr3:69873800-69887600 Weak transcription NHLF lung
4 chr3:69876400-69881200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr3:69879400-69881800 Weak transcription Fetal Heart heart
6 chr3:69879600-69884200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr3:69879600-69886000 Weak transcription Right Atrium heart
8 chr3:69879600-69886000 Weak transcription Skeletal Muscle Female skeletal muscle
9 chr3:69881000-69881200 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
10 chr3:69881000-69881200 Genic enhancers Ovary ovary
11 chr3:69881000-69881200 Enhancers Pancreas Pancrea
12 chr3:69881000-69881200 Enhancers K562 blood
13 chr3:69881000-69881400 Enhancers Brain Hippocampus Middle brain
14 chr3:69881000-69881400 Enhancers Left Ventricle heart
15 chr3:69881000-69881600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
16 chr3:69881000-69881600 Enhancers Psoas Muscle Psoas
17 chr3:69881000-69881600 Enhancers Right Ventricle heart

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