Variant report

Variant rs4709632
Chromosome Location chr6:162909935-162909936
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:162907000-162912400 Weak transcription Left Ventricle heart
2 chr6:162907000-162915000 Weak transcription Fetal Muscle Leg muscle
3 chr6:162907400-162931400 Weak transcription Psoas Muscle Psoas
4 chr6:162907600-162910000 Weak transcription Fetal Brain Male brain
5 chr6:162907600-162914600 Weak transcription Fetal Stomach stomach
6 chr6:162907600-162916000 Weak transcription Rectal Smooth Muscle rectum
7 chr6:162909400-162910600 Enhancers HepG2 liver
8 chr6:162909400-162912000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
9 chr6:162909600-162923200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
10 chr6:162909800-162910400 Flanking Active TSS Liver Liver
11 chr6:162909800-162912400 Weak transcription Pancreas Pancrea
12 chr6:162909800-162912600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
13 chr6:162909800-162922000 Weak transcription Aorta Aorta

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