chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1205778169205778173TTTG42GENIChomozygous127476431
1205783831205783832AG60GENIChomozygous108515517
1205780823205780824AG61GENIChomozygous108515513
1205782782205782783AG57GENIChomozygous108515514
1205783066205783067TA40GENIChomozygous108515515
1205783216205783217TC59GENIChomozygous108515516
1205783841205783842GA62GENIChomozygous108515518
1205784212205784213AG50GENIChomozygous108515519
1205784348205784349TC62GENIChomozygous108515520
1205784700205784701A30GENIChomozygous127476432
1205784723205784724CA43GENIChomozygous108515521
1205785019205785020CG50GENIChomozygous108515522
1205785948205785948C50GENIChomozygous127476433
1205787279205787309GCTGTGTCCCTTGTGTAGACAGGCATGCTG30GENIChomozygous127476434
1205788631205788632TC53GENIChomozygous108515530
1205785504205785505CT54GENIChomozygous108515523
1205785568205785569TC46GENIChomozygous108515524
1205786087205786088AG48GENIChomozygous108515525
1205787562205787563CT59GENIChomozygous108515527
1205787607205787608AT62GENIChomozygous108515528
1205787622205787623GA55GENIChomozygous108515529
1205789330205789331TG43GENIChomozygous108515531
1205789682205789683GA55GENIChomozygous108515532