chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7123364778123364779CCGGCG2GENIChomozygous54089721
7123365023123365024GC15GENIChomozygous54089726
7123365036123365037T-16GENIChomozygous54089727
7123367556123367557CCA3GENICheterozygous54089736
7123378139123378140GGACAC10GENICheterozygous55003300
7123378139123378140GGACACACAC10GENICpossibly homozygous55003302
7123379970123379971TTC11GENICheterozygous55003304
7123402604123402605CCAAAA8GENICheterozygous55003306
7123402605123402606A-8GENICheterozygous55003308
7123391261123391262T-19GENICheterozygous54587250
7123405589123405590CCA8GENICheterozygous55003310
7123405590123405591A-8GENICheterozygous55003312
7123415518123415519GT12GENIChomozygous54921438
7123419981123419982GGTTTTTTTTTTTTTTTTTTTTTTT6GENIChomozygous55003314
7123421452123421453GGTT4GENICheterozygous54089907