chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1254726985254726986TC26GENIChomozygous108616442
1254727030254727031GA32GENIChomozygous109022349
1254727125254727126CT23GENIChomozygous109022350
1254727903254727904GA22GENIChomozygous109022351
1254728031254728032CA12GENIChomozygous109022352
1254729488254729489CA13GENIChomozygous108616447
1254728603254728644GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGACAG4GENIChomozygous135289481
1254729571254729574GGA13GENIChomozygous127504855
1254729648254729656GGAGGGAG18GENIChomozygous132542367
1254729699254729700GA17GENIChomozygous109022353
1254729707254729708GA20GENIChomozygous109022354
1254729715254729716GA22GENIChomozygous109022355
1254729835254729836CT23GENIChomozygous108616449
1254729915254729916TA26GENIChomozygous109022356
1254729916254729917TA26GENIChomozygous109022357
1254729928254729928A25GENIChomozygous132542368
1254730229254730230CA20GENIChomozygous108616451
1254730310254730311TC17GENIChomozygous108616452
1254730634254730635GA16GENIChomozygous109022358
1254730950254730951TC23GENIChomozygous108616453
1254731582254731583GT20GENICpossibly homozygous108616454
1254731989254731990CG18GENIChomozygous108616456
1254732480254732481GA17GENIChomozygous109022359
1254733154254733155AC15GENIChomozygous108616457
1254733280254733281GA16GENIChomozygous108616458
1254734061254734061ATATAT14GENIChomozygous132542369
1254734152254734153AG19GENIChomozygous109022360
1254734249254734250TG22GENIChomozygous108616459
1254735243254735244GA18GENIChomozygous109022361
1254729691254729692GA18GENIChomozygous132558469
1254734811254734812GA27GENIChomozygous109213679
1254737111254737112T18GENIChomozygous132542370
1254737626254737627TC3GENIChomozygous134663430
1254737629254737630TC3GENIChomozygous134663431
1254737632254737633TC3GENIChomozygous134663432