Variant report

Variant rs60190856
Chromosome Location chr16:70885508-70885509
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr16:70880800-70906600 Weak transcription Fetal Kidney kidney
2 chr16:70881200-70886400 Weak transcription Fetal Heart heart
3 chr16:70882800-70892000 Weak transcription Brain Cingulate Gyrus brain
4 chr16:70883000-70885600 Weak transcription Fetal Lung lung
5 chr16:70883800-70885600 Weak transcription Brain Hippocampus Middle brain
6 chr16:70883800-70902200 Weak transcription Fetal Brain Male brain
7 chr16:70883800-70904200 Weak transcription Pancreas Pancrea
8 chr16:70883800-70906400 Weak transcription Brain Substantia Nigra brain
9 chr16:70884400-70889200 Weak transcription Brain Germinal Matrix brain
10 chr16:70884400-70898800 Weak transcription Brain Anterior Caudate brain
11 chr16:70884400-70898800 Weak transcription Brain Inferior Temporal Lobe brain
12 chr16:70884400-70899800 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
13 chr16:70884600-70902000 Weak transcription Brain Angular Gyrus brain
14 chr16:70885000-70885600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr16:70885000-70887800 Enhancers HMEC breast
16 chr16:70885000-70888200 Enhancers NHEK skin
17 chr16:70885400-70885600 Enhancers K562 blood
18 chr16:70885400-70888000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin

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