Variant report

Variant rs9495974
Chromosome Location chr6:141681449-141681450
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:141680800-141681600 Flanking Active TSS H9 Derived Neuron Cultured Cells ES cell derived
2 chr6:141680800-141682000 Enhancers Cortex derived primary cultured neurospheres brain
3 chr6:141681000-141681600 Active TSS Aorta Aorta
4 chr6:141681000-141681600 Enhancers Fetal Brain Male brain
5 chr6:141681000-141681600 Enhancers Fetal Heart heart
6 chr6:141681200-141681600 Flanking Active TSS H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
7 chr6:141681200-141681600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr6:141681200-141681600 Flanking Active TSS Brain Germinal Matrix brain
9 chr6:141681200-141681600 Flanking Active TSS Fetal Brain Female brain
10 chr6:141681200-141681600 Flanking Active TSS Pancreatic Islets Pancreatic Islet
11 chr6:141681200-141681600 Enhancers Ovary ovary
12 chr6:141681200-141681600 Active TSS Right Atrium heart
13 chr6:141681200-141681600 Enhancers NHDF-Ad bronchial

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