chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1262038874262038875CT16GENICheterozygous61817030
1262039436262039437AC16GENICheterozygous61182468
1262039533262039534TC24GENICheterozygous61638765
1262039615262039616CCTATATA12GENICheterozygous61638766
1262039629262039630GGTGTA13GENICheterozygous61182469
1262040405262040406CT10GENICheterozygous61182470
1262040531262040532TG20GENICheterozygous61182471
1262041205262041206CT17GENICheterozygous61638767
1262041696262041697GC29GENICheterozygous61182472
1262042006262042007GGAA11GENICheterozygous61182475
1262042103262042104CA16GENICheterozygous61182476
1262042735262042736AG20GENICheterozygous61182477
1262043051262043052CT20GENICheterozygous61638768
1262043375262043376AG23GENICheterozygous61182478
1262043456262043457GT14GENICheterozygous61182479
1262043752262043753CCT8GENICheterozygous61638769
1262043769262043770AT9GENICheterozygous61638770
1262043770262043771AT9GENICheterozygous61638771
1262043850262043851GA9GENICheterozygous61182481
1262044092262044095CCT---9GENICheterozygous61182486
1262044197262044198GT14GENICheterozygous61182487
1262044890262044891TC10GENICheterozygous61182489
1262045098262045099T-7GENICheterozygous61182492
1262045620262045622TT--9GENICheterozygous61182495
1262045654262045655GT16GENICheterozygous61638778
1262045782262045783CT19GENICheterozygous61638779
1262046560262046561GA13GENICheterozygous61638780
1262046655262046656CT10GENICheterozygous61638781