chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5154781784154781785TA13GENIChomozygous114062623
5154782235154782236CT11GENIChomozygous114062625
5154782437154782438GA23GENIChomozygous114062627
5154782441154782442AC23GENIChomozygous114062629
5154782501154782502AG20GENIChomozygous114062631
5154782502154782503AC21GENIChomozygous114062633
5154783139154783140GC27GENIChomozygous114062635
5154783365154783366AC22GENIChomozygous114062637
5154783602154783603TC30GENIChomozygous114062639
5154784154154784155GA19GENIChomozygous114062641
5154784267154784268TG24GENIChomozygous114062643
5154784480154784481GA25GENIChomozygous114062645
5154784899154784900GA14GENIChomozygous114062647
5154785091154785092CT15GENIChomozygous114062651
5154787043154787044CT9GENIChomozygous114062653
5154789553154789554CT23GENIChomozygous114062657
5154789557154789558TC21GENIChomozygous114062659
5154795006154795007AG20GENIChomozygous114062669
5154796471154796472CT21GENIChomozygous114062671
5154797275154797276GT24GENIChomozygous114062673
5154797804154797805GA21GENIChomozygous114062675
5154799267154799268GA25GENIChomozygous114062677
5154799292154799293GA23GENIChomozygous114062679
5154799962154799963TA14GENIChomozygous114062681
5154800016154800017TG18GENIChomozygous114062683