chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1174082190174082191AG1GENIChomozygous60949187
1174082247174082248AG7GENIChomozygous60949188
1174082304174082305TC12GENIChomozygous60949189
1174082879174082880TC8GENIChomozygous60949190
1174082930174082931CT18GENIChomozygous60949191
1174082983174082984CT19GENICheterozygous60949192
1174083007174083008AG14GENICpossibly homozygous60949193
1174083049174083050TA2GENIChomozygous60949194
1174083065174083066CG8GENICpossibly homozygous60949195
1174083374174083375G-6GENIChomozygous60949196
1174085558174085559TC3GENICheterozygous60949201
1174086687174086688CT5GENIChomozygous60949202
1174087021174087022CT11GENIChomozygous60949203
1174087554174087555CT18GENIChomozygous60949204
1174087601174087602CT22GENICpossibly homozygous60949205
1174087743174087744GA21GENICpossibly homozygous60949206