chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171796814317968144GA33GENIChomozygous805095300
171796841817968419CT13GENIChomozygous805095301
171797053117970532TC12GENIChomozygous805095302
171797325017973251AG23GENIChomozygous805095303
171797365017973651CT13GENIChomozygous805095304
171797477917974780TC14GENIChomozygous805095305
171797486817974869AC15GENIChomozygous805095306
171797520817975209AT14GENIChomozygous805095307
171797596217975963CT27GENIChomozygous805095308
171797674417976745CT18GENIChomozygous805095309
171797729417977295GA23GENIChomozygous805095310
171797954517979546GA19GENIChomozygous805095311
171798042217980423AG20GENIChomozygous805095312
171798045517980456CT22GENIChomozygous805095313
171798152117981522CT13GENIChomozygous805095314
171798257417982575AG15GENIChomozygous805095315
171798306917983070AG15GENICpossibly homozygous805095316
171798420117984202AG17GENIChomozygous805095317
171798440217984403GA25GENIChomozygous805095318
171798462917984630AT11GENIChomozygous805095319
171798500017985001GA24GENIChomozygous805095320
171798569117985692AG8GENIChomozygous805095321
171798670717986708CT20GENICpossibly homozygous805095322
171798775917987760GT22GENIChomozygous805095323