Variant report

Variant rs16988014
Chromosome Location chr20:25726034-25726035
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:25708000-25731400 Weak transcription Esophagus oesophagus
2 chr20:25713400-25731000 Weak transcription Left Ventricle heart
3 chr20:25714400-25731200 Weak transcription Pancreas Pancrea
4 chr20:25715600-25731400 Weak transcription Aorta Aorta
5 chr20:25721000-25731000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr20:25724400-25727000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
7 chr20:25724400-25731400 Weak transcription Brain Angular Gyrus brain
8 chr20:25725400-25726200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr20:25725400-25726200 Enhancers NHEK skin
10 chr20:25725400-25727800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
11 chr20:25726000-25731200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr20:25726000-25731400 Weak transcription HMEC breast

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