chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4143066632143066633AG23GENIChomozygous674165405
4143067173143067174TA32GENIChomozygous674165406
4143067462143067463AG25GENIChomozygous674165407
4143067604143067605CT33GENICpossibly homozygous674165408
4143067911143067912TC27GENIChomozygous674165409
4143068188143068191CGT---27GENIChomozygous770617456
4143068398143068399CT20GENIChomozygous674165410
4143068496143068497GA23GENIChomozygous674165411
4143068696143068697AG31GENICpossibly homozygous674165412
4143068742143068743AG25GENICpossibly homozygous674165413
4143068973143068975TT--23GENICheterozygous770617458
4143068974143068975T-23GENICpossibly homozygous770617459
4143068982143068983TC24GENIChomozygous674165414
4143069523143069524AC20GENICpossibly homozygous674165415
4143070410143070411CT26GENICpossibly homozygous674165416
4143070429143070430TC26GENICpossibly homozygous674165417
4143070847143070848AG33GENICpossibly homozygous674165418
4143070907143070908GT29GENIChomozygous674165419
4143071028143071029CA21GENIChomozygous674165420
4143071303143071304GT20GENICpossibly homozygous674165421
4143071608143071609GA32GENIChomozygous674165422
4143071742143071743AC33GENIChomozygous674165423