chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1193340307193340308GT21GENIChomozygous108469894
1193344438193344439GA38GENIChomozygous108469895
1193345276193345277AG19GENIChomozygous108469897
1193347670193347671CT22GENIChomozygous108469899
1193347750193347751GT31GENIChomozygous108469900
1193349649193349650GT29GENIChomozygous108469902
1193351535193351536GA27GENIChomozygous108469903
1193357499193357500GA27GENIChomozygous108469905
1193369283193369284AG23GENIChomozygous108469908
1193369975193369976TC32GENIChomozygous108469910
1193370284193370285AG26GENIChomozygous108469911
1193370339193370340CT34GENIChomozygous108469913
1193370447193370448CA34GENIChomozygous108469915
1193370534193370535GA34GENICpossibly homozygous108469916
1193370612193370613GT34GENIChomozygous108469918
1193371036193371037TG24GENIChomozygous108469920
1193371468193371469TC24GENIChomozygous108469923
1193371586193371587CT26GENIChomozygous108469925
1193371596193371597CT28GENIChomozygous108469926
1193371627193371628GC32GENIChomozygous108469928
1193371816193371817TC17GENIChomozygous108469929
1193371995193371996GT34GENIChomozygous108469931
1193372091193372092AC20GENIChomozygous108469933
1193372566193372567CT22GENIChomozygous108469934
1193373336193373337GC37GENIChomozygous108469936
1193373650193373651GA29GENIChomozygous120475257
1193375786193375787GT35GENIChomozygous108469937
1193378683193378684TG23GENIChomozygous108469939
1193383764193383765AG35GENIChomozygous108469944
1193383787193383788CT36GENIChomozygous108469945
1193385126193385127CG18GENIChomozygous108469947
1193387962193387963CA26GENIChomozygous108469949
1193389233193389234TC22GENIChomozygous108469950
1193390327193390328AT25GENIChomozygous108469952
1193390431193390432CT14GENIChomozygous108469954
1193390508193390509TC17GENIChomozygous108469955
1193391481193391482CG23GENIChomozygous108469957