chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
16574188065741881CT6GENIChomozygous125523558
16574261865742619GA15GENIChomozygous125523559
16574295865742959GA17GENIChomozygous125523560
16574312865743129AG21GENIChomozygous125523561
16574316265743163GA28GENIChomozygous125523562
16574319265743193GA16GENIChomozygous125523563
16574359065743591GA17GENIChomozygous125523564
16574376865743769GC16GENIChomozygous125523565
16574551565745516AC15GENIChomozygous125479885
16574598565745986GT14GENIChomozygous125523566
16574612165746122CA15GENIChomozygous125523567
16574639265746393CG8GENIChomozygous125479887
16574652465746525GA15GENIChomozygous125523568
16574703465747035TC24GENIChomozygous125523569
16574770965747710TC18GENIChomozygous125523570
16574774865747749AT16GENIChomozygous125523571
16574792465747925AG5GENIChomozygous125523572
16574804465748045AG13GENIChomozygous125523573
16574871465748715TC13GENIChomozygous125523574
16574880465748805AG20GENIChomozygous125523575
16574926765749268TG9GENIChomozygous125523576
16574989465749895AG17GENIChomozygous125523577
16574997465749975CT15GENIChomozygous125523578
16575010065750101GA12GENIChomozygous125479889
16575096165750962AC25GENIChomozygous125523579
16575122865751229CT11GENIChomozygous125523580
16575349165753492TC4GENICheterozygous125523581
16575445465754455TG13GENIChomozygous125479895
16575686865756869TC23GENIChomozygous125523582