chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7122150594122150595GC45GENIChomozygous54087457
7122150826122150827CCCA5GENICheterozygous54087458
7122152648122152649GC56GENICheterozygous54087459
7122152761122152762GA85GENICheterozygous54087460
7122152842122152843TA68GENICheterozygous54087461
7122153042122153043TC71GENICheterozygous54087462
7122153558122153559GA40GENIChomozygous54087463
7122155179122155180CT11GENICheterozygous54087464
7122155180122155181AAG7GENIChomozygous54087465
7122155864122155865TC91GENICpossibly homozygous54087466
7122156186122156187CT70GENICheterozygous54087467
7122156212122156213AG70GENICheterozygous54087468
7122156360122156361TC80GENICheterozygous54087469
7122156620122156621T-3GENIChomozygous54511065
7122156951122156952AT65GENIChomozygous54087471
7122157951122157952CT35GENIChomozygous54087472
7122158468122158469CT47GENIChomozygous54087473
7122158658122158659TC37GENIChomozygous54087474
7122158661122158662AG40GENIChomozygous54087475
7122173519122173531GTTTGTTTGTTT------------12GENIChomozygous54087478