chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2210778065210778066CA37GENIChomozygous110223584
2210778578210778579GA25GENIChomozygous110223585
2210778806210778807CA19GENIChomozygous110223586
2210778858210778859TC19GENIChomozygous110223587
2210779046210779047AG16GENIChomozygous110223588
2210779476210779477CT16GENIChomozygous110223589
2210780245210780246GA29GENIChomozygous110223590
2210780827210780828AG19GENIChomozygous110223591
2210781063210781064TC13GENICpossibly homozygous110223592
2210781838210781839AG19GENIChomozygous110223595
2210782126210782127GA27GENIChomozygous110223596