chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71106954011069541AAAG3GENICheterozygous55070631
71107022711070228TC15GENIChomozygous53787298
71107044511070446TA20GENIChomozygous53787303
71107061011070611CT18GENIChomozygous53787304
71107073011070731GC30GENIChomozygous53787305
71107093211070944AAAAAAAAAAAA------------17GENICpossibly homozygous53787306
71107106511071066GA12GENIChomozygous53787307
71107115711071164TAAGCGC-------1GENIChomozygous53787308
71107117911071180GGAGATTTAGCTCAGTGGT1GENIChomozygous54954276
71107123011071231GGAA5GENIChomozygous53787310
71107136811071369AT13GENIChomozygous53787311
71107139511071396GA17GENIChomozygous53787312
71107190211071903TC20GENIChomozygous53787313
71107190611071907AG21GENIChomozygous53787314
71107204711072048AG13GENIChomozygous53787315
71107224511072246GA17GENIChomozygous53787316
71107239811072399AG17GENIChomozygous53787317
71107242811072429CG19GENICpossibly homozygous53787318
71107242911072430AG20GENICpossibly homozygous53787319
71107252511072526CT15GENIChomozygous53787320
71107263811072639TC2GENIChomozygous53787322
71107275611072758AC--3GENICheterozygous53787328
71107279711072798GGA2GENIChomozygous54884810
71107285411072855AC1GENIChomozygous53787331
71107288411072885AG2GENICheterozygous53787332
71107288711072888AG2GENICheterozygous53787333
71107289111072892TC2GENICheterozygous53787334
71107289411072895TC2GENIChomozygous53787335
71107291911072920C-4GENIChomozygous53787336
71107293711072938CT8GENIChomozygous54884812
71107293911072940AC9GENIChomozygous54884814
71107295911072960AC10GENIChomozygous53787338
71107305611073057GA7GENIChomozygous53787339
71107307011073071AAC6GENIChomozygous53787340
71107319511073196TC8GENIChomozygous53787341
71107324011073241AG8GENIChomozygous53787342
71107328511073286CT10GENIChomozygous53787343
71107330311073304AG9GENIChomozygous53787344
71107372311073724CG26GENICheterozygous53787354
71107375311073754TC24GENIChomozygous53787355
71107396711073968CT17GENIChomozygous53787357
71107323911073240GA8GENIChomozygous54710171