chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5156998341156998342TC16GENIChomozygous71175626
5157001539157001540AT28GENIChomozygous71175630
5157003741157003742TC28GENIChomozygous71175636
5157007249157007250CT29GENIChomozygous71175638
5157008772157008773TC29GENIChomozygous71175642
5157008773157008774TC29GENIChomozygous71175644
5157011380157011381TC18GENIChomozygous72246302
5157001637157001638CT17GENIChomozygous72246272
5157002342157002343TA21GENIChomozygous72246275
5157003504157003505AG30GENIChomozygous72246279
5157004117157004118GC34GENIChomozygous72246283
5157004660157004661TC22GENIChomozygous72246287
5157009119157009120TA27GENIChomozygous72246291
5157011213157011214TG28GENIChomozygous72246295
5157011316157011317GA12GENIChomozygous72246298
5157008425157008426AG19GENICpossibly homozygous72459512
5157011489157011490AG22GENIChomozygous71175646
5157011615157011616TC18GENIChomozygous72246306
5157011986157011987GA20GENIChomozygous72246310
5157012258157012259TC11GENIChomozygous72246314
5157013421157013422GA22GENIChomozygous72246317
5157013990157013991GC40GENIChomozygous72246321
5157016024157016025TG33GENIChomozygous72246325
5157016329157016330TC26GENIChomozygous72246329
5157017008157017009GA23GENIChomozygous72246333
5157017454157017455AG21GENIChomozygous71175660
5157018585157018586GA13GENIChomozygous72246337
5157019113157019114AG8GENIChomozygous71175676
5157019227157019228AG7GENIChomozygous72459517
5157019545157019546AG21GENIChomozygous72246341
5157021880157021881CG23GENIChomozygous71175680
5157022306157022307CT25GENIChomozygous72246343
5157022527157022528CT14GENIChomozygous72246347
5157022575157022576TC16GENIChomozygous71175684
5157023064157023065AG33GENIChomozygous71175688
5157023295157023296AG11GENIChomozygous71175690