Variant report

Variant esv1849493
Chromosome Location chr4:31065510-31068042
allele n/a
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:31056800-31066000 Weak transcription Fetal Heart heart
2 chr4:31058000-31077200 Weak transcription Aorta Aorta
3 chr4:31064000-31066800 Weak transcription Pancreatic Islets Pancreatic Islet
4 chr4:31064600-31066000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
5 chr4:31066000-31066400 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr4:31066000-31066400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
7 chr4:31066000-31066600 Enhancers Fetal Heart heart
8 chr4:31066000-31067000 Enhancers Left Ventricle heart
9 chr4:31066400-31088600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
10 chr4:31066600-31069200 Weak transcription Fetal Heart heart
11 chr4:31066800-31067200 Active TSS Pancreatic Islets Pancreatic Islet
12 chr4:31067000-31067200 Enhancers iPS-18 Cell Line embryonic stem cell
13 chr4:31067200-31067400 Flanking Active TSS Pancreatic Islets Pancreatic Islet
14 chr4:31067200-31070800 Weak transcription iPS-18 Cell Line embryonic stem cell
15 chr4:31067400-31067800 Enhancers Pancreatic Islets Pancreatic Islet
16 chr4:31067800-31073400 Weak transcription Pancreatic Islets Pancreatic Islet

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