chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1226901504226901505CT27GENIChomozygous108998474
1226901576226901577AG39GENIChomozygous108998475
1226901578226901579AG38GENIChomozygous108998476
1226902153226902154GA23GENIChomozygous108998478
1226902717226902718GA33GENIChomozygous109198301
1226902763226902764AG25GENIChomozygous108998479
1226903070226903071CT10GENIChomozygous108998480
1226903978226903979GA24GENIChomozygous108998481
1226904568226904569TA24GENIChomozygous109198303
1226904816226904817TC27GENIChomozygous108998482
1226905207226905208TC43GENIChomozygous108998483
1226905620226905621CT14GENIChomozygous108998485
1226905666226905667TG18GENIChomozygous108998486
1226906302226906303GC28GENIChomozygous108998487
1226906577226906578TC29GENIChomozygous108998488
1226906872226906873CA23GENIChomozygous108998489
1226907193226907194GA25GENIChomozygous108998490
1226907259226907260GT20GENIChomozygous108998491
1226908443226908444CT16GENIChomozygous108998492
1226908748226908749TC11GENIChomozygous108998494
1226909496226909497AG17GENIChomozygous108998495
1226909547226909548TC30GENIChomozygous108998496
1226909627226909628GA33GENIChomozygous109198309
1226909815226909816CT27GENIChomozygous108998497
1226910809226910810AG19GENIChomozygous108998498
1226911126226911127AG22GENIChomozygous109198313
1226911576226911577GA22GENIChomozygous109198315
1226911751226911752TC13GENIChomozygous108998499
1226912037226912038CT21GENIChomozygous108998501