chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
153739794737397948T-24GENIChomozygous48502802
153739884537398846AG12GENIChomozygous48502806
153740169037401691GA27GENIChomozygous48502808
153740219537402196TC20GENIChomozygous48502810
153740304837403049GA16GENIChomozygous48502812
153740314537403146GGAA18GENIChomozygous48502814
153740460937404610AG13GENIChomozygous48502818
153740473437404735TC18GENIChomozygous48502820
153740494237404943A-10GENIChomozygous48502822
153740566737405668G-7GENIChomozygous48502824
153740688937406891GT--9GENIChomozygous49048687
153740842837408429CA17GENIChomozygous48502829
153740853937408540GT16GENIChomozygous48502831
153740868037408681GA24GENICpossibly homozygous48502833
153741043137410432AATT17GENIChomozygous48502837
153741086537410873GTGACACG--------11GENIChomozygous48502839
153741178037411781T-8GENICheterozygous48502843
153741179737411798AG9GENIChomozygous48502845
153741180937411810TC9GENIChomozygous48502847
153741253937412540CT15GENIChomozygous48502849
153741299837412999GGCTCT10GENIChomozygous48502853
153741306537413066CT11GENIChomozygous48502855
153741332637413327GT20GENIChomozygous48502857
153741415337414154AC23GENIChomozygous48502859