chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2240626970240626971CG51GENIChomozygous110334626
2240627877240627878GC92GENICpossibly homozygous111184490
2240629350240629351TC70GENIChomozygous110334630
2240629028240629029AG35GENICpossibly homozygous110632336
2240629035240629036CT44GENIChomozygous110632338
2240629475240629476TC79GENIChomozygous110334632
2240630554240630555CA77GENIChomozygous110334636
2240633212240633213AT69GENIChomozygous110334642
2240634732240634733CT48GENIChomozygous111184494
2240635309240635310CT68GENIChomozygous111184496
2240637131240637132CA67GENIChomozygous111184498
2240639969240639969T55GENICpossibly homozygous127754209
2240630972240630973T69GENIChomozygous127754205
2240631792240631793GT55GENIChomozygous111289883
2240631792240631792T55GENIChomozygous132810219
2240635657240635657T49GENIChomozygous132810220
2240640189240640189T62GENIChomozygous132810221
2240642780240642781GT56GENIChomozygous110334662
2240645839240645840GA60GENIChomozygous110334666
2240646082240646083GA42GENIChomozygous110334668
2240646879240646880GT65GENIChomozygous111184502
2240647025240647026CT67GENIChomozygous111184504
2240647378240647378T78GENIChomozygous132810222
2240649590240649591GA59GENIChomozygous111184506
2240650792240650792T75GENICpossibly homozygous132810223
2240652974240652975GT50GENIChomozygous111184508