Variant report

Variant rs6749096
Chromosome Location chr2:212616720-212616721
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:7 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:212610200-212626600 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
2 chr2:212616200-212616800 Enhancers Brain Germinal Matrix brain
3 chr2:212616200-212617200 Enhancers HUVEC blood vessel
4 chr2:212616400-212616800 Enhancers Right Ventricle heart
5 chr2:212616400-212617000 Enhancers Fetal Heart heart
6 chr2:212616600-212616800 Enhancers Psoas Muscle Psoas
7 chr2:212616600-212617000 Enhancers Fetal Lung lung

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