Variant report

Variant rs78632168
Chromosome Location chr9:105617531-105617532
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:2 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:105616800-105619000 Enhancers Fetal Heart heart
2 chr9:105617200-105618000 Weak transcription Placenta Amnion Placenta Amnion

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