chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1181475751181475752CT48GENIChomozygous143804612
1181483704181483705TC54GENIChomozygous143804614
1181486502181486503A30GENICheterozygous403547251
1181486151181486152TC59GENIChomozygous135763222
1181486501181486502A28GENICpossibly homozygous403547249
1181486501181486502AT28GENICheterozygous403547250
1181486502181486503AT30GENICheterozygous403547252
1181486503181486504A31GENICheterozygous403547253
1181486503181486504AT31GENICheterozygous403547254
1181488392181488393AG42GENIChomozygous135763223
1181489843181489844TC54GENIChomozygous135763224
1181492107181492108CT38GENIChomozygous143804616
1181494318181494319GA57GENIChomozygous143804617
1181486648181486649CT47GENIChomozygous145315972
1181494595181494595CT60GENIChomozygous143744480
1181492937181492938T45GENIChomozygous135449030