Variant report

Variant rs4748460
Chromosome Location chr10:18698576-18698577
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 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 chr10:18690200-18713000 Weak transcription Ovary ovary
4 chr10:18690600-18702800 Weak transcription Stomach Smooth Muscle stomach
5 chr10:18691000-18698600 Weak transcription Fetal Intestine Large intestine
6 chr10:18691000-18702600 Weak transcription Pancreas Pancrea
7 chr10:18692000-18702600 Weak transcription Liver Liver
8 chr10:18692000-18712600 Weak transcription Cortex derived primary cultured neurospheres brain
9 chr10:18692400-18703000 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
10 chr10:18692600-18702800 Weak transcription Brain Inferior Temporal Lobe brain
11 chr10:18692600-18707600 Weak transcription Brain Angular Gyrus brain
12 chr10:18695400-18699400 Weak transcription Pancreatic Islets Pancreatic Islet
13 chr10:18696400-18702800 Weak transcription Right Ventricle heart
14 chr10:18697400-18699000 Strong transcription Fetal Adrenal Gland Adrenal Gland
15 chr10:18698000-18699200 Enhancers Left Ventricle heart
16 chr10:18698400-18698800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
17 chr10:18698400-18699200 Genic enhancers Fetal Heart heart

Quick Search:


  
Input of quick search could be:

what's new

Quick links