chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1211249147211249148CA20GENIChomozygous948966298
1211249164211249165AG24GENIChomozygous948966299
1211249514211249515AG19GENIChomozygous948966300
1211249867211249868GA26GENIChomozygous948966301
1211249879211249880GT25GENIChomozygous948966302
1211250193211250194AC22GENIChomozygous948966303
1211250496211250497TC14GENIChomozygous948966304
1211250622211250623CG12GENIChomozygous948966305
1211250623211250624CT12GENIChomozygous948966306
1211250700211250701GA23GENIChomozygous948966307
1211252203211252204AG24GENIChomozygous948966308
1211252276211252277CT7GENIChomozygous948966309
1211252677211252678CT8GENIChomozygous948966310
1211254276211254277AC21GENIChomozygous948966311
1211254477211254478TC14GENIChomozygous948966312
1211254496211254497CT14GENIChomozygous948966313
1211255440211255441GT23GENIChomozygous948966314
1211255616211255617AT20GENIChomozygous948966315
1211256722211256723TC21GENIChomozygous948966316
1211257074211257075AG26GENIChomozygous948966317
1211258234211258235GA25GENIChomozygous948966318
1211258541211258542CT20GENIChomozygous948966319
1211258803211258804TC25GENIChomozygous948966320
1211259737211259738AG18GENIChomozygous948966321
1211259868211259869CT19GENIChomozygous948966322
1211260475211260476CG14GENIChomozygous948966323
1211261011211261012GA39GENIChomozygous948966324
1211261278211261279AG23GENIChomozygous948966325
1211261430211261431CT26GENIChomozygous948966326
1211261727211261728CT15GENIChomozygous948966327
1211262253211262254CT14GENIChomozygous948966328
1211262513211262514GA9GENIChomozygous948966329
1211262865211262866AG16GENIChomozygous948966330
1211263517211263518CA27GENICpossibly homozygous948966331
1211264098211264099TG21GENIChomozygous948966332
1211264888211264889CA13GENIChomozygous948966333
1211264889211264890TA13GENIChomozygous948966334