chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2210778065210778066CA57GENICpossibly homozygous110223584
2210778578210778579GA55GENICpossibly homozygous110223585
2210778806210778807CA50GENIChomozygous110223586
2210778858210778859TC52GENIChomozygous110223587
2210779046210779047AG45GENIChomozygous110223588
2210779476210779477CT50GENIChomozygous110223589
2210780245210780246GA40GENIChomozygous110223590
2210780827210780828AG45GENIChomozygous110223591
2210781063210781064TC61GENIChomozygous110223592
2210781761210781762TC45GENIChomozygous110908886
2210781838210781839AG58GENIChomozygous110223595
2210782126210782127GA54GENIChomozygous110223596
2210782758210782759GA53GENIChomozygous110908887