Variant report

Variant rs12102972
Chromosome Location chr16:70918958-70918959
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr16:70904200-70920600 Weak transcription Colon Smooth Muscle Colon
2 chr16:70907000-70919800 Weak transcription Fetal Kidney kidney
3 chr16:70908800-70933400 Weak transcription Fetal Brain Male brain
4 chr16:70911800-70919200 Weak transcription Pancreas Pancrea
5 chr16:70911800-70920000 Strong transcription Fetal Brain Female brain
6 chr16:70912400-70919400 Strong transcription Brain Germinal Matrix brain
7 chr16:70913000-70920200 Strong transcription Brain Anterior Caudate brain
8 chr16:70916400-70921200 Weak transcription Fetal Intestine Small intestine
9 chr16:70916800-70919200 Weak transcription Brain Substantia Nigra brain
10 chr16:70917000-70919000 Weak transcription Spleen Spleen
11 chr16:70917200-70919800 Weak transcription Breast Myoepithelial Primary Cells Breast
12 chr16:70918200-70920200 Weak transcription Brain Hippocampus Middle brain
13 chr16:70918400-70920400 Strong transcription Brain Inferior Temporal Lobe brain
14 chr16:70918600-70919600 Strong transcription Brain Angular Gyrus brain
15 chr16:70918600-70919600 Strong transcription Brain Cingulate Gyrus brain
16 chr16:70918800-70919200 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland
17 chr16:70918800-70919600 Strong transcription Pancreatic Islets Pancreatic Islet
18 chr16:70918800-70919800 Strong transcription Brain Dorsolateral Prefrontal Cortex brain
19 chr16:70918800-70920000 ZNF genes & repeats Aorta Aorta

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