chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5169925888169925889TC17GENIChomozygous56086504
5169926647169926648TTAAA9GENIChomozygous56086505
5169926842169926843GGT10GENICpossibly homozygous55838300
5169926950169926951TTAACAAC9GENIChomozygous56086506
5169926987169926988TC16GENIChomozygous56086507
5169927039169927044AGGGA-----6GENICheterozygous55838301
5169927043169927044AAG6GENICheterozygous55838302
5169927232169927233GGA9GENIChomozygous56086508
5169927369169927370GA20GENIChomozygous56086509
5169927552169927553AG22GENIChomozygous56086510
5169927640169927641TC22GENIChomozygous56086511
5169927711169927712AT7GENIChomozygous56086512
5169927908169927909GGCA20GENIChomozygous56086513
5169928102169928103GA18GENIChomozygous56086514
5169928315169928317TT--10GENIChomozygous56086515
5169928348169928349CT12GENIChomozygous56086516
5169929426169929427TA24GENIChomozygous56086517
5169929427169929428TA24GENIChomozygous56086518
5169929573169929574AG24GENIChomozygous56086519
5169929891169929892AG29GENIChomozygous56086520