chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1183733699183733700GA21GENIChomozygous108971654
1183733749183733750AG18GENIChomozygous108442933
1183734692183734693TC18GENIChomozygous108442937
1183734739183734740TC13GENIChomozygous108442939
1183735704183735705GA10GENIChomozygous108442941
1183736381183736382TC20GENIChomozygous108971655
1183736851183736852TC25GENIChomozygous108442943
1183736969183736970AG13GENIChomozygous108442945
1183737389183737390AG16GENIChomozygous108442947
1183738108183738109GA17GENIChomozygous108971656
1183738671183738672TC15GENIChomozygous108442949
1183739329183739330CT24GENIChomozygous108971657
1183739776183739777AG20GENIChomozygous108442953
1183741251183741252TC27GENIChomozygous108971658
1183742205183742206GA17GENIChomozygous108971659
1183742219183742220GA16GENIChomozygous108971660
1183742233183742234AC21GENIChomozygous108442959
1183742619183742620GA9GENIChomozygous108971661
1183743163183743164TC20GENIChomozygous108442961
1183743563183743564TC14GENIChomozygous108971662
1183743752183743753TC15GENIChomozygous108442963
1183743929183743930CG20GENICpossibly homozygous108442965
1183744306183744307CA10GENIChomozygous108442967