chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1266866964266866965TG81GENIChomozygous778810487
1266867306266867307GA51GENIChomozygous778810488
1266868398266868399CT45GENICpossibly homozygous778810489
1266869171266869172TC61GENIChomozygous778810490
1266871799266871800AG74GENIChomozygous778810491
1266875024266875025GT52GENICpossibly homozygous778810492
1266876378266876379AG77GENIChomozygous778810493
1266878148266878149GA60GENIChomozygous778810494
1266879795266879796TG57GENIChomozygous778810495
1266881721266881722AG48GENIChomozygous778810496
1266884218266884219CT63GENICpossibly homozygous778810497
1266885897266885898TC57GENIChomozygous778810498
1266885968266885969CT48GENICpossibly homozygous778810499
1266886214266886215TG61GENICheterozygous778810500
1266886406266886407TG67GENICheterozygous778810501
1266886425266886426CT58GENICheterozygous778810502
1266886438266886439TG73GENICheterozygous778810503
1266886538266886539GT108GENICheterozygous778810504
1266886559266886560TG87GENICheterozygous778810505
1266886577266886578TG84GENICheterozygous778810506
1266886676266886677TG14GENICheterozygous778810507
1266886685266886686TG18GENICheterozygous778810508
1266886856266886857TG59GENICheterozygous778810509
1266886928266886929TG98GENICheterozygous778810510
1266892788266892789TC32GENICpossibly homozygous778810511
1266894775266894776GA48GENIChomozygous778810512
1266895476266895477AG65GENIChomozygous778810513
1266897388266897389TC71GENIChomozygous778810514
1266897681266897682GA41GENIChomozygous778810515