chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1166112744166112745AG24GENIChomozygous108356099
1166112767166112768GA23GENIChomozygous108356100
1166112971166112972TC25GENIChomozygous108356101
1166114044166114045AT19GENIChomozygous108356103
1166115991166115992CT22GENIChomozygous108954689
1166118009166118010AC26GENIChomozygous108356107
1166118917166118918CT24GENIChomozygous108954690
1166119551166119552CT28GENIChomozygous108954691
1166119761166119762GC18GENIChomozygous108954692
1166120611166120612TC20GENIChomozygous108356110
1166122867166122868CT15GENIChomozygous108954693
1166123068166123069TA19GENICpossibly homozygous108954694
1166125176166125177CT32GENIChomozygous108954695
1166126608166126609GA30GENIChomozygous108954696
1166129034166129035GA24GENIChomozygous108954697
1166130094166130095TC17GENIChomozygous108356119
1166130239166130240AG27GENIChomozygous108356120
1166130647166130648GA32GENIChomozygous108356122
1166130856166130857CA28GENIChomozygous108356123
1166131697166131698AT28GENIChomozygous108954698
1166136898166136899GA27GENIChomozygous108954699