chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4153352599153352600CA35GENIChomozygous56988394
4153353289153353290CG23GENIChomozygous58475430
4153355340153355341TC22GENIChomozygous56988401
4153355636153355637GGA14GENICheterozygous56988404
4153355637153355638A-14GENICpossibly homozygous58347358
4153359291153359292AG33GENIChomozygous56988419
4153360177153360179TT--8GENIChomozygous58475442
4153360656153360657GA32GENIChomozygous56988422
4153362723153362724GC35GENIChomozygous56988435
4153365684153365685A-22GENIChomozygous56988448
4153366811153366813AA--16GENICheterozygous59132348
4153364465153364468TTT---19GENIChomozygous57521560
4153355747153355751GTTT----21GENIChomozygous59132340
4153362914153362915GA32GENIChomozygous59132342
4153364236153364237TC31GENIChomozygous59132344
4153366321153366322AC32GENIChomozygous59132346
4153366812153366813A-16GENICpossibly homozygous58475454
4153367025153367026CT35GENIChomozygous59132350
4153367920153367921CT29GENIChomozygous56988454
4153369045153369046AG30GENIChomozygous59132352
4153369113153369114TC41GENIChomozygous56988458
4153369222153369223TC35GENIChomozygous56988459
4153369259153369260GGA10GENIChomozygous57843427
4153369274153369275AG19GENIChomozygous56988461
4153370586153370587CA34GENIChomozygous56988462
4153371222153371223GA36GENIChomozygous56988464