chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5156998341156998342TC24GENIChomozygous71175626
5157001539157001540AT17GENIChomozygous71175630
5157003741157003742TC14GENIChomozygous71175636
5157007249157007250CT23GENIChomozygous71175638
5157008772157008773TC24GENIChomozygous71175642
5157008773157008774TC24GENIChomozygous71175644
5157011489157011490AG19GENIChomozygous71175646
5157011615157011616TC23GENIChomozygous72246306
5157001637157001638CT17GENIChomozygous72246272
5157002342157002343TA18GENIChomozygous72246275
5157003504157003505AG31GENIChomozygous72246279
5157004117157004118GC15GENIChomozygous72246283
5157004660157004661TC14GENIChomozygous72246287
5157009119157009120TA31GENICpossibly homozygous72246291
5157011213157011214TG16GENIChomozygous72246295
5157011316157011317GA17GENIChomozygous72246298
5157011380157011381TC20GENICpossibly homozygous72246302
5157008425157008426AG13GENICheterozygous72459512
5157011986157011987GA20GENIChomozygous72246310
5157012258157012259TC17GENIChomozygous72246314
5157013421157013422GA8GENIChomozygous72246317
5157013990157013991GC10GENIChomozygous72246321
5157016024157016025TG25GENIChomozygous72246325
5157016329157016330TC22GENIChomozygous72246329
5157017008157017009GA18GENIChomozygous72246333
5157017454157017455AG13GENIChomozygous71175660
5157018585157018586GA22GENIChomozygous72246337
5157019113157019114AG12GENIChomozygous71175676
5157019227157019228AG17GENIChomozygous72459517
5157019545157019546AG20GENIChomozygous72246341
5157021880157021881CG19GENIChomozygous71175680
5157022306157022307CT25GENIChomozygous72246343
5157022527157022528CT16GENIChomozygous72246347
5157022575157022576TC10GENIChomozygous71175684
5157023064157023065AG16GENIChomozygous71175688
5157023295157023296AG17GENIChomozygous71175690