Variant report

Variant rs9970145
Chromosome Location chr1:180575322-180575323
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:180564800-180579600 Weak transcription Right Atrium heart
2 chr1:180568200-180579800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr1:180569800-180575400 Weak transcription Pancreatic Islets Pancreatic Islet
4 chr1:180573400-180578400 Weak transcription Pancreas Pancrea
5 chr1:180573400-180578800 Weak transcription Fetal Heart heart
6 chr1:180573400-180578800 Weak transcription HMEC breast
7 chr1:180573400-180578800 Weak transcription NHEK skin
8 chr1:180573400-180579000 Weak transcription Left Ventricle heart
9 chr1:180573800-180578800 Weak transcription Breast Myoepithelial Primary Cells Breast
10 chr1:180574600-180575600 Enhancers HUES48 Cell Line embryonic stem cell
11 chr1:180574600-180575800 Enhancers Cortex derived primary cultured neurospheres brain
12 chr1:180574800-180576000 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
13 chr1:180575000-180575400 Weak transcription K562 blood
14 chr1:180575000-180575800 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
15 chr1:180575000-180576000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived

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