Variant report

Variant rs11014091
Chromosome Location chr10:18695328-18695329
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:18690000-18703600 Weak transcription Fetal Stomach stomach
2 chr10:18690000-18705600 Weak transcription Aorta Aorta
3 chr10:18690200-18695800 Weak transcription Right Ventricle heart
4 chr10:18690200-18698000 Weak transcription Left Ventricle heart
5 chr10:18690200-18713000 Weak transcription Ovary ovary
6 chr10:18690600-18702800 Weak transcription Stomach Smooth Muscle stomach
7 chr10:18691000-18698600 Weak transcription Fetal Intestine Large intestine
8 chr10:18691000-18702600 Weak transcription Pancreas Pancrea
9 chr10:18692000-18702600 Weak transcription Liver Liver
10 chr10:18692000-18712600 Weak transcription Cortex derived primary cultured neurospheres brain
11 chr10:18692400-18703000 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
12 chr10:18692600-18702800 Weak transcription Brain Inferior Temporal Lobe brain
13 chr10:18692600-18707600 Weak transcription Brain Angular Gyrus brain
14 chr10:18693400-18696800 Enhancers Fetal Heart heart
15 chr10:18694000-18695400 Enhancers Pancreatic Islets Pancreatic Islet
16 chr10:18694800-18695400 Enhancers HUES6 Cell Line embryonic stem cell
17 chr10:18695000-18695400 Enhancers iPS-18 Cell Line embryonic stem cell
18 chr10:18695200-18696000 Strong transcription Fetal Adrenal Gland Adrenal Gland

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