chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4147534547147534548GA8GENIChomozygous56973464
4147535446147535447CT10GENIChomozygous57347209
4147536531147536532AG17GENIChomozygous56973466
4147537037147537038CG18GENIChomozygous57347211
4147537454147537455CT21GENIChomozygous57347213
4147539026147539027GT16GENIChomozygous57347215
4147540061147540062GA18GENIChomozygous57347217
4147540753147540754GC19GENIChomozygous57347219
4147544186147544187CCA7GENIChomozygous57347223
4147544683147544684CG8GENIChomozygous57347225
4147544826147544827AG21GENIChomozygous56973493
4147545754147545755CT18GENIChomozygous57347229
4147549828147549829AG9GENIChomozygous56973499
4147550435147550436GA12GENIChomozygous57347231
4147550534147550535TC9GENIChomozygous56973501
4147556689147556690AC7GENIChomozygous56973515
4147557812147557813TC12GENIChomozygous56973516
4147562506147562507GA9GENIChomozygous57347235
4147567643147567644AG19GENIChomozygous56973526
4147569684147569685TA13GENIChomozygous56973529
4147576706147576707TC10GENIChomozygous56973540
4147579621147579622TC14GENIChomozygous56973543
4147584731147584732TC21GENIChomozygous56973553
4147584806147584807GA11GENIChomozygous57347241
4147586609147586610CT11GENIChomozygous57347242