chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1226900376226900377GC4GENIChomozygous108998473
1226901024226901025AG21GENIChomozygous125409934
1226901504226901505CT34GENIChomozygous108998474
1226901576226901577AG32GENIChomozygous108998475
1226901578226901579AG31GENIChomozygous108998476
1226901955226901956GA34GENIChomozygous108998477
1226902116226902116T40GENIChomozygous130833728
1226902153226902154GA42GENIChomozygous108998478
1226902291226902291CA36GENIChomozygous130833729
1226903070226903071CT31GENIChomozygous108998480
1226903978226903979GA36GENIChomozygous108998481
1226904816226904817TC55GENIChomozygous108998482
1226905207226905208TC47GENIChomozygous108998483
1226905239226905240AT45GENIChomozygous108998484
1226905620226905621CT36GENIChomozygous108998485
1226905666226905667TG46GENICpossibly homozygous108998486
1226905905226905905TG32GENIChomozygous130833730
1226906302226906303GC37GENIChomozygous108998487
1226906577226906578TC51GENIChomozygous108998488
1226906872226906873CA47GENIChomozygous108998489
1226907193226907194GA45GENIChomozygous108998490
1226907259226907260GT51GENIChomozygous108998491
1226907466226907466C33GENICpossibly homozygous134653214
1226908144226908144GG38GENICpossibly homozygous134653215
1226908443226908444CT55GENIChomozygous108998492
1226908593226908594CT59GENICpossibly homozygous108998493
1226908748226908749TC56GENIChomozygous108998494
1226909496226909497AG42GENIChomozygous108998495
1226909547226909548TC48GENIChomozygous108998496
1226910809226910810AG42GENIChomozygous108998498
1226911751226911752TC46GENIChomozygous108998499
1226912082226912085GGT42GENICpossibly homozygous131263739
1226912191226912191T49GENIChomozygous131263740
1226911807226911808CG40GENIChomozygous108998500
1226912037226912038CT54GENIChomozygous108998501