chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2168264252168264253CT27GENIChomozygous141419445
2168267583168267584G21GENICpossibly homozygous403026575
2168266364168266365GC21GENIChomozygous136363707
2168267579168267580GC21GENICheterozygous154004514
2168267581168267582GC21GENICheterozygous154004515
2168267583168267584GC21GENICheterozygous154004516
2168267579168267580G21GENICpossibly homozygous403026573
2168267581168267582G21GENICpossibly homozygous403026574
2168267585168267586GC21GENICheterozygous154004517
2168267585168267586G21GENICpossibly homozygous403026576
2168267587168267588GC21GENICheterozygous154004518
2168267587168267588G21GENICpossibly homozygous403026577
2168267599168267600GC21GENICpossibly homozygous154004519
2168267599168267600G21GENICheterozygous403026578
2168267601168267602GC24GENIChomozygous403026579
2168267601168267602G24GENICheterozygous403026580
2168267603168267604GC24GENIChomozygous141419446
2168267605168267606GC24GENIChomozygous141419447
2168267607168267608GC25GENIChomozygous141419448
2168268779168268780GA18GENIChomozygous141419449
2168269768168269769CT18GENIChomozygous136363708
2168272620168272621CT15GENIChomozygous141419450
2168270273168270273A3GENIChomozygous144279962