chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4153352599153352600CA3GENICheterozygous56988394
4153353289153353290CG19GENICpossibly homozygous58475430
4153355340153355341TC20GENICpossibly homozygous56988401
4153355636153355637GGA3GENICheterozygous56988404
4153355747153355751GTTT----3GENIChomozygous59132340
4153359291153359292AG8GENIChomozygous56988419
4153360656153360657GA5GENICheterozygous56988422
4153362723153362724GC10GENIChomozygous56988435
4153362914153362915GA11GENIChomozygous59132342
4153364236153364237TC18GENIChomozygous59132344
4153365684153365685A-6GENIChomozygous56988448
4153366321153366322AC14GENICpossibly homozygous59132346
4153366812153366813A-1GENIChomozygous58475454
4153367025153367026CT22GENIChomozygous59132350
4153367920153367921CT17GENIChomozygous56988454
4153369045153369046AG30GENIChomozygous59132352
4153369113153369114TC21GENICpossibly homozygous56988458
4153369222153369223TC8GENIChomozygous56988459
4153369274153369275AG1GENIChomozygous56988461
4153364465153364468TTT---6GENICheterozygous57521560
4153355637153355638A-3GENICheterozygous58347358
4153370586153370587CA19GENICpossibly homozygous56988462