Variant report

Variant rs16826126
Chromosome Location chr3:156152008-156152009
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:156111200-156161600 Weak transcription Aorta Aorta
2 chr3:156147400-156157200 Weak transcription Rectal Smooth Muscle rectum
3 chr3:156148400-156153400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr3:156148600-156153200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr3:156149800-156153600 Enhancers NHEK skin
6 chr3:156150000-156153600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr3:156150800-156152200 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
8 chr3:156150800-156160600 Weak transcription Duodenum Smooth Muscle Duodenum
9 chr3:156151000-156152200 Enhancers HUVEC blood vessel
10 chr3:156151000-156152800 Weak transcription Esophagus oesophagus
11 chr3:156151400-156152600 Weak transcription HMEC breast
12 chr3:156152000-156152200 Enhancers Pancreas Pancrea
13 chr3:156152000-156152200 Bivalent Enhancer NHDF-Ad bronchial

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