chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1205780823205780824AG26GENIChomozygous108515513
1205782782205782783AG35GENIChomozygous108515514
1205783066205783067TA34GENIChomozygous108515515
1205783216205783217TC24GENIChomozygous108515516
1205783831205783832AG19GENIChomozygous108515517
1205783841205783842GA23GENIChomozygous108515518
1205784212205784213AG16GENIChomozygous108515519
1205784348205784349TC20GENIChomozygous108515520
1205784731205784732AC5GENIChomozygous120817715
1205785019205785020CG34GENIChomozygous108515522
1205785504205785505CT36GENIChomozygous108515523
1205785568205785569TC25GENIChomozygous108515524
1205786087205786088AG29GENIChomozygous108515525
1205787562205787563CT22GENIChomozygous108515527
1205787607205787608AT24GENIChomozygous108515528
1205787622205787623GA20GENIChomozygous108515529
1205788631205788632TC39GENIChomozygous108515530
1205789330205789331TG38GENIChomozygous108515531
1205789682205789683GA26GENIChomozygous108515532