Variant report

Variant rs56371106
Chromosome Location chr14:104819867-104819868
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:104816800-104820400 Weak transcription Fetal Brain Male brain
2 chr14:104817400-104820000 Weak transcription Brain Germinal Matrix brain
3 chr14:104817600-104820400 Weak transcription Fetal Lung lung
4 chr14:104819600-104820200 Weak transcription Left Ventricle heart
5 chr14:104819600-104820400 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell
6 chr14:104819600-104820400 Enhancers Spleen Spleen
7 chr14:104819600-104820800 Bivalent Enhancer Right Ventricle heart
8 chr14:104819800-104820400 ZNF genes & repeats Lung lung
9 chr14:104819800-104821000 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
10 chr14:104819800-104822000 Bivalent Enhancer Fetal Stomach stomach

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