chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135607491856074919TC28GENIChomozygous642729523
135607497056074971CCAGAG29GENIChomozygous752747314
135607519556075196GA17GENIChomozygous642729524
135607522056075230ACACACACAC----------6GENIChomozygous752747315
135607526356075264TG16GENIChomozygous642729525
135607538756075388A-19GENIChomozygous752747317
135608191456081915AG31GENIChomozygous642729526
135608208256082083GA35GENIChomozygous642729527
135608239756082398C-26GENIChomozygous752747318
135608260856082609TC30GENIChomozygous642729528
135608269256082693TC17GENIChomozygous642729529
135608276256082763TTCC10GENICheterozygous752747320
135608276256082763TTCCC10GENICpossibly homozygous752747321
135608311156083112GA26GENIChomozygous642729530
135608376556083766GA31GENIChomozygous642729531
135608391756083918AT33GENIChomozygous642729532
135608402856084029GGTGTA6GENICheterozygous752747322
135608412656084127CA24GENIChomozygous642729533
135608442356084424CT27GENICpossibly homozygous642729534
135608451756084518CCTTT15GENIChomozygous752747325
135608481956084820CG27GENIChomozygous642729535
135608504756085048AT28GENIChomozygous642729536
135608527856085279GA24GENIChomozygous642729537
135608534956085350AG17GENIChomozygous642729538
135608555056085551AG29GENIChomozygous642729539
135608582756085828CG31GENIChomozygous642729540
135608608256086083CT31GENIChomozygous642729541
135608623656086237TC25GENIChomozygous642729542
135608629256086293GGAC36GENIChomozygous752747326