chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1420666182066619AG10GENICpossibly homozygous48447578
1420690062069007CA14GENICpossibly homozygous48447579
1420694592069460CG14GENIChomozygous48447580
1420702932070294GA19GENIChomozygous48447582
1420708872070888AG6GENIChomozygous48447583
1420725862072587AG13GENIChomozygous48447584
1420726612072662GA14GENICpossibly homozygous48447585
1420728312072832GA11GENICheterozygous48447586
1420728532072854CT4GENIChomozygous48447587
1420730292073030CCT13GENIChomozygous48447588
1420738122073813GA16GENIChomozygous48447590
1420741362074137AG13GENICpossibly homozygous48447591
1420742102074211CT6GENICheterozygous48447592
1420743462074347GA6GENIChomozygous48447593
1420744112074412CT4GENIChomozygous48447594
1420747392074740TC12GENIChomozygous48447595
1420760112076012TC12GENIChomozygous48447596
1420786332078634AG10GENIChomozygous48447597
1420788332078834GA12GENIChomozygous48447598
1420788452078846A-14GENIChomozygous48447599