chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1226901024226901025AG11GENIChomozygous125409934
1226901504226901505CT15GENIChomozygous108998474
1226901576226901577AG19GENIChomozygous108998475
1226901578226901579AG19GENIChomozygous108998476
1226901955226901956GA15GENIChomozygous108998477
1226902116226902116T26GENIChomozygous130833728
1226902153226902154GA23GENIChomozygous108998478
1226902291226902291CA19GENIChomozygous130833729
1226904816226904817TC27GENIChomozygous108998482
1226902763226902764AG19GENIChomozygous108998479
1226903070226903071CT28GENIChomozygous108998480
1226903978226903979GA23GENIChomozygous108998481
1226902717226902718GA16GENIChomozygous109198301
1226904568226904569TA17GENIChomozygous109198303
1226905207226905208TC26GENIChomozygous108998483
1226905239226905240AT24GENIChomozygous108998484
1226905620226905621CT21GENIChomozygous108998485
1226905666226905667TG25GENIChomozygous108998486
1226906302226906303GC23GENIChomozygous108998487
1226906577226906578TC22GENIChomozygous108998488
1226906872226906873CA23GENIChomozygous108998489
1226907193226907194GA24GENIChomozygous108998490
1226907259226907260GT16GENIChomozygous108998491
1226908443226908444CT21GENIChomozygous108998492
1226908593226908594CT23GENIChomozygous108998493
1226908748226908749TC13GENIChomozygous108998494
1226909496226909497AG28GENIChomozygous108998495
1226909547226909548TC25GENIChomozygous108998496
1226909627226909628GA20GENIChomozygous109198309
1226909815226909816CT21GENICpossibly homozygous108998497
1226910809226910810AG13GENIChomozygous108998498
1226910988226910989TA18GENIChomozygous109198311
1226911126226911127AG26GENIChomozygous109198313
1226911576226911577GA30GENIChomozygous109198315
1226911751226911752TC29GENIChomozygous108998499
1226911807226911808CG28GENIChomozygous108998500
1226912037226912038CT28GENIChomozygous108998501
1226911006226911007GC21GENICpossibly homozygous131283006
1226912082226912085GGT31GENIChomozygous131263739
1226912191226912191T26GENIChomozygous131263740