chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1181475751181475752CT35GENIChomozygous143804612
1181483704181483705TC29GENIChomozygous143804614
1181486151181486152TC63GENIChomozygous135763222
1181486501181486502A29GENICpossibly homozygous403547249
1181486501181486502AT29GENICheterozygous403547250
1181486502181486503A28GENICheterozygous403547251
1181486502181486503AT28GENICheterozygous403547252
1181486648181486649CT46GENIChomozygous145315972
1181488392181488393AG33GENIChomozygous135763223
1181489843181489844TC37GENIChomozygous135763224
1181492107181492108CT57GENIChomozygous143804616
1181494318181494319GA34GENIChomozygous143804617
1181494595181494595CT55GENICpossibly homozygous143744480
1181492937181492938T42GENIChomozygous135449030