chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2051792755179276GT10GENIChomozygous63740562
2051792775179278TG10GENIChomozygous63717868
2051817765181777AG50GENIChomozygous63343469
2051840855184086CT41GENIChomozygous63717869
2051881885188189TC57GENIChomozygous63343474
2051888545188855AC73GENIChomozygous63343477
2051895125189513TC41GENIChomozygous63717870
2051867305186731TC6GENICheterozygous63758688
2051870355187036GA61GENICpossibly homozygous63758689
2051911395191140CG11GENICheterozygous63758690
2051926405192641TG54GENIChomozygous63717871
2051956805195681GA45GENIChomozygous63717872
2051973385197339GA73GENIChomozygous63343499
2051996775199678CG34GENIChomozygous63643423
2052013685201369CG51GENIChomozygous63343503
2052020395202040AG53GENIChomozygous63343505
2052057815205782AG61GENICpossibly homozygous63343509