chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1264060117264060118AG46GENIChomozygous792600359
1264060439264060440AG35GENICpossibly homozygous792600360
1264061026264061027AG28GENIChomozygous792600361
1264061283264061284GA34GENIChomozygous792600362
1264061466264061467TC39GENIChomozygous792600363
1264062297264062298TC37GENICpossibly homozygous792600364
1264062501264062502AG40GENIChomozygous792600365
1264062532264062533CT38GENIChomozygous792600366
1264062601264062602CT50GENIChomozygous792600367
1264062947264062948GA43GENICpossibly homozygous792600368
1264064003264064004AG27GENIChomozygous792600369
1264064234264064235TG26GENICpossibly homozygous792600370
1264064641264064642CT35GENIChomozygous792600371
1264064988264064989AG33GENIChomozygous792600372
1264065091264065092TC40GENIChomozygous792600373
1264065424264065425CA46GENIChomozygous792600374
1264065813264065814AT40GENIChomozygous792600375
1264066698264066699TC51GENIChomozygous792600376
1264066832264066833GA44GENIChomozygous792600377
1264066841264066842CT41GENIChomozygous792600378
1264067060264067061TC35GENIChomozygous792600379
1264067293264067294AG40GENIChomozygous792600380
1264067967264067968CT26GENICpossibly homozygous792600381
1264068063264068064TC25GENIChomozygous792600382
1264069621264069622CT37GENICpossibly homozygous792600383
1264069737264069738CT42GENICpossibly homozygous792600384
1264069747264069748GA42GENICpossibly homozygous792600385
1264070790264070791CT44GENIChomozygous792600386
1264071386264071387GA35GENIChomozygous792600387
1264071462264071463CA40GENIChomozygous792600388