chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7124394187124394188CT28GENIChomozygous116226677
7124394297124394298GA44GENIChomozygous115865802
7124394939124394940CT33GENIChomozygous115865804
7124397390124397391CT37GENIChomozygous115865806
7124397833124397834CT26GENIChomozygous115865808
7124398464124398465CT31GENIChomozygous116226678
7124399200124399201TG46GENIChomozygous115865810
7124399486124399487TC38GENIChomozygous115865812
7124399730124399731GA30GENIChomozygous115865814
7124400939124400940TG31GENIChomozygous115865818
7124400960124400961AG33GENIChomozygous116226679
7124401027124401028CT24GENIChomozygous116226680
7124401057124401058AG26GENIChomozygous116226681
7124401280124401281TG30GENIChomozygous115865822
7124401381124401382CT27GENIChomozygous116226682
7124401820124401821TG29GENIChomozygous115865828
7124402426124402427AG29GENIChomozygous115865832
7124402503124402504CT23GENIChomozygous116082904
7124402652124402653GC40GENIChomozygous116226683
7124403350124403351GA35GENIChomozygous116226684
7124403900124403901TC6GENIChomozygous116263014
7124405633124405634GA25GENIChomozygous116226688
7124405645124405646CG26GENIChomozygous116226689
7124406768124406769TC33GENIChomozygous116082933
7124407058124407059AG19GENIChomozygous116082935
7124408155124408156AG29GENIChomozygous115865850
7124408715124408716AG15GENIChomozygous115865852
7124409397124409398TC26GENIChomozygous115865854
7124409645124409646CA27GENIChomozygous115865856