chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10109838211109838212CT12GENIChomozygous51600252
10109838439109838440GT15GENIChomozygous51957803
10109838578109838579TA27GENIChomozygous51600257
10109838605109838606TG30GENIChomozygous51600259
10109839116109839117GA30GENIChomozygous52272468
10109839348109839349CG37GENIChomozygous51957806
10109839507109839508TC35GENIChomozygous51600266
10109839553109839554AG36GENIChomozygous51600267
10109839568109839569AG42GENIChomozygous51600268
10109839639109839640CT38GENIChomozygous51957809
10109840050109840051TC27GENIChomozygous51957812
10109840612109840613GA37GENIChomozygous51957815
10109840618109840619CT37GENIChomozygous51957818
10109841754109841755CT35GENIChomozygous51600276
10109841944109841945GA16GENIChomozygous51600277
10109842164109842165GA34GENIChomozygous52272470
10109842575109842576GA39GENIChomozygous52272472
10109844912109844913AG26GENIChomozygous51600281
10109843612109843615AAA---14GENIChomozygous52410125
10109843616109843637AAAGAAAGAAAGAAAAAAAGA---------------------14GENIChomozygous52410127
10109845672109845673CCTTTT2GENICheterozygous52410129
10109845672109845673CCTTTTTTT2GENICheterozygous52410131