chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1226901504226901505CT27GENIChomozygous108998474
1226901576226901577AG34GENIChomozygous108998475
1226901578226901579AG34GENIChomozygous108998476
1226902153226902154GA20GENIChomozygous108998478
1226902717226902718GA43GENIChomozygous109198301
1226902763226902764AG35GENIChomozygous108998479
1226903070226903071CT8GENIChomozygous108998480
1226903978226903979GA20GENIChomozygous108998481
1226904568226904569TA28GENIChomozygous109198303
1226904816226904817TC20GENIChomozygous108998482
1226905207226905208TC48GENIChomozygous108998483
1226905239226905240AT51GENICpossibly homozygous108998484
1226905620226905621CT22GENIChomozygous108998485
1226905666226905667TG21GENIChomozygous108998486
1226906302226906303GC24GENIChomozygous108998487
1226906577226906578TC38GENIChomozygous108998488
1226906872226906873CA45GENIChomozygous108998489
1226907193226907194GA40GENIChomozygous108998490
1226907259226907260GT38GENIChomozygous108998491
1226908443226908444CT32GENIChomozygous108998492
1226908593226908594CT32GENIChomozygous108998493
1226908748226908749TC45GENIChomozygous108998494
1226909496226909497AG36GENIChomozygous108998495
1226909547226909548TC31GENIChomozygous108998496
1226909815226909816CT46GENIChomozygous108998497
1226910809226910810AG32GENIChomozygous108998498
1226911126226911127AG25GENIChomozygous109198313
1226911576226911577GA36GENIChomozygous109198315
1226911751226911752TC42GENIChomozygous108998499
1226911807226911808CG46GENIChomozygous108998500
1226912037226912038CT33GENIChomozygous108998501