Variant report

Variant rs28700881
Chromosome Location chr16:70887071-70887072
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr16:70880800-70906600 Weak transcription Fetal Kidney kidney
2 chr16:70882800-70892000 Weak transcription Brain Cingulate Gyrus brain
3 chr16:70883800-70902200 Weak transcription Fetal Brain Male brain
4 chr16:70883800-70904200 Weak transcription Pancreas Pancrea
5 chr16:70883800-70906400 Weak transcription Brain Substantia Nigra brain
6 chr16:70884400-70889200 Weak transcription Brain Germinal Matrix brain
7 chr16:70884400-70898800 Weak transcription Brain Anterior Caudate brain
8 chr16:70884400-70898800 Weak transcription Brain Inferior Temporal Lobe brain
9 chr16:70884400-70899800 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
10 chr16:70884600-70902000 Weak transcription Brain Angular Gyrus brain
11 chr16:70885000-70887800 Enhancers HMEC breast
12 chr16:70885000-70888200 Enhancers NHEK skin
13 chr16:70885400-70888000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
14 chr16:70885600-70887800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr16:70886400-70887200 Weak transcription Aorta Aorta
16 chr16:70886400-70887600 Enhancers Placenta Amnion Placenta Amnion
17 chr16:70887000-70887800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin

Quick Search:


  
Input of quick search could be:

what's new

Quick links