chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3163790922163790923AG19GENIChomozygous111805201
3163795849163795850GA18GENIChomozygous111805205
3163796543163796544AT18GENIChomozygous111805207
3163801941163801942TA23GENIChomozygous111805209
3163802432163802433AC17GENIChomozygous111805211
3163802904163802905GC22GENIChomozygous111805213
3163804950163804951TC19GENIChomozygous111805215
3163807928163807929CG14GENIChomozygous111805217
3163807985163807986CT20GENIChomozygous111805219
3163811948163811949CT18GENIChomozygous111805225
3163812018163812019GA28GENIChomozygous111805227
3163812659163812660TA11GENIChomozygous111805229
3163813856163813857TC20GENIChomozygous111805233
3163817918163817919AG5GENIChomozygous111805237
3163818521163818522TC11GENIChomozygous111805239
3163818576163818577CT20GENIChomozygous111805241
3163818705163818706AG12GENIChomozygous111805243
3163819225163819226CT3GENICheterozygous125841508
3163819286163819287CG5GENIChomozygous111805245
3163823432163823433AG17GENIChomozygous111805247
3163825638163825639CT6GENIChomozygous111805254
3163827464163827465CT16GENICheterozygous111805258
3163829069163829070GC7GENIChomozygous111805260
3163830900163830901TC7GENIChomozygous111805262
3163840060163840061AG20GENIChomozygous111805268
3163840805163840806GA30GENICpossibly homozygous111805274
3163842859163842860TC13GENIChomozygous111805278
3163843264163843265CT10GENIChomozygous111805280
3163845395163845396CT19GENIChomozygous111805282
3163846500163846501TC16GENIChomozygous111805284
3163846545163846546AT16GENIChomozygous111805286
3163846616163846617AG22GENIChomozygous111805288
3163846689163846690GA22GENIChomozygous125841510
3163846849163846850GA7GENIChomozygous125841511
3163847474163847475TA27GENIChomozygous111805290
3163831580163831581GT8GENICheterozygous125985707