chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109544285095442851GA19GENICheterozygous53560847
109544319695443197CT20GENICheterozygous53560848
109544348495443485A-16GENICheterozygous53560849
109544414495444145CT10GENICheterozygous53560850
109544439495444395TC13GENICheterozygous53560851
109544448895444491ATT---20GENICheterozygous53560852
109544497895444979AG26GENICheterozygous53560853
109544499395444994CT21GENICheterozygous53560854
109544508295445083GA15GENICheterozygous53560855
109544511495445115GA17GENICheterozygous53560856
109544538095445381GA18GENICheterozygous53560857
109544553995445540CA12GENICheterozygous53560858
109544768295447683GA9GENICheterozygous53560859
109544854595448546TC15GENICheterozygous53560860
109544973095449731GA26GENICheterozygous51551444
109544990995449910AG17GENICheterozygous53560861
109545053395450534AT12GENICheterozygous53560862
109545123695451237GA19GENICheterozygous53560863
109545178795451788GA12GENIChomozygous51551445
109545178895451789TC12GENIChomozygous51551446
109545187595451876AAGCCCG10GENICheterozygous51551447
109545461395454614T-15GENICheterozygous51551451
109545527395455274GA17GENICheterozygous53560864
109545535295455353CT14GENICheterozygous53560865
109545678695456787GA18GENICheterozygous51551456
109545787395457874C-16GENICheterozygous51551457
109545831095458311GA20GENICheterozygous53560866
109545905495459055CT10GENICheterozygous53560867