chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1189946015189946020ACATT29GENIChomozygous131580084
1189946622189946622A26GENIChomozygous131580085
1189948198189948199CG18GENIChomozygous109176582
1189950782189950783TC34GENIChomozygous108464552
1189951616189951617TC22GENIChomozygous109176584
1189953256189953257GA31GENIChomozygous109176586
1189953557189953558CG24GENIChomozygous109176588
1189954947189954948AC20GENIChomozygous108464554
1189955338189955340AC21GENIChomozygous131580086
1189955458189955459AC24GENIChomozygous108464555
1189956369189956372CCC26GENIChomozygous131580087
1189957838189957839GA19GENIChomozygous109176590
1189958630189958631AG30GENIChomozygous108977089
1189959414189959415CT16GENIChomozygous109176592
1189959752189959753GA21GENIChomozygous108464557
1189956849189956850T28GENICpossibly homozygous130732189
1189960048189960049AC14GENIChomozygous108464558
1189960023189960023AA16GENIChomozygous127466336
1189960038189960039A14GENIChomozygous127466337
1189960056189960057T13GENIChomozygous127466338
1189956372189956373CA26GENIChomozygous120781649
1189960066189960066G11GENIChomozygous127466339