chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1166112744166112745AG29GENIChomozygous108356099
1166112767166112768GA28GENIChomozygous108356100
1166112971166112972TC28GENIChomozygous108356101
1166113512166113513TC20GENIChomozygous109436561
1166114044166114045AT10GENIChomozygous108356103
1166116805166116806TC24GENIChomozygous109436563
1166116998166116999CT18GENICpossibly homozygous109436565
1166118009166118010AC26GENIChomozygous108356107
1166120611166120612TC21GENIChomozygous108356110
1166121584166121585CT27GENIChomozygous109436567
1166128174166128175GA17GENIChomozygous109436569
1166130094166130095TC19GENIChomozygous108356119
1166130239166130240AG28GENIChomozygous108356120
1166130647166130648GA23GENIChomozygous108356122
1166130856166130857CA22GENIChomozygous108356123
1166138201166138202GA16GENIChomozygous109436577
1166129132166129133CT21GENIChomozygous109436571
1166135074166135075TG19GENIChomozygous109436573
1166137623166137624GA17GENIChomozygous109436575