chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4121392163121392164TC26GENIChomozygous112824770
4121392170121392171GC25GENIChomozygous112824772
4121392175121392176TC25GENIChomozygous112824774
4121392210121392211TC28GENIChomozygous112824776
4121392217121392218GC24GENIChomozygous112824778
4121392221121392222TC24GENIChomozygous112824780
4121392231121392232CT23GENIChomozygous112824782
4121392256121392257CG27GENIChomozygous112824784
4121431660121431661AC27GENIChomozygous112824790
4121431858121431859GT5GENIChomozygous112824792
4121435836121435837GA18GENIChomozygous112824794
4121469071121469072CT22GENIChomozygous113155211
4121470020121470021AG24GENIChomozygous113155212
4121470296121470297CT28GENIChomozygous113155213
4121472012121472013GA16GENICheterozygous112824812
4121473568121473569AG57GENICheterozygous113241064
4121510044121510045CT5GENIChomozygous112824814
4121543978121543979TC15GENICheterozygous113241065