chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1183733749183733750AG46GENIChomozygous108442933
1183734692183734693TC40GENIChomozygous108442937
1183734739183734740TC35GENIChomozygous108442939
1183735051183735052TG51GENIChomozygous109358702
1183735704183735705GA47GENIChomozygous108442941
1183736851183736852TC51GENIChomozygous108442943
1183736969183736970AG57GENIChomozygous108442945
1183737389183737390AG48GENICpossibly homozygous108442947
1183738671183738672TC45GENICpossibly homozygous108442949
1183738782183738783AG50GENIChomozygous109358704
1183739507183739508TC38GENIChomozygous109358706
1183739776183739777AG47GENIChomozygous108442953
1183740454183740455GA52GENIChomozygous109358708
1183741837183741838CA49GENICheterozygous108762676
1183741838183741839GA47GENICheterozygous108762677
1183741868183741869TC51GENICheterozygous108762678
1183741995183741996TC16GENIChomozygous108442957
1183742219183742220GA27GENIChomozygous108971660
1183742233183742234AC23GENIChomozygous108442959
1183743163183743164TC57GENIChomozygous108442961
1183743752183743753TC48GENIChomozygous108442963
1183743929183743930CG50GENIChomozygous108442965
1183744306183744307CA39GENIChomozygous108442967