chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5156998341156998342TC23GENIChomozygous71175626
5157001539157001540AT20GENIChomozygous71175630
5157001637157001638CT17GENIChomozygous72246272
5157002342157002343TA22GENIChomozygous72246275
5157003504157003505AG32GENIChomozygous72246279
5157003741157003742TC15GENICpossibly homozygous71175636
5157004117157004118GC19GENIChomozygous72246283
5157007249157007250CT29GENICpossibly homozygous71175638
5157008772157008773TC32GENIChomozygous71175642
5157008773157008774TC32GENIChomozygous71175644
5157011213157011214TG19GENIChomozygous72246295
5157011316157011317GA14GENIChomozygous72246298
5157011380157011381TC16GENIChomozygous72246302
5157011489157011490AG16GENIChomozygous71175646
5157011615157011616TC26GENIChomozygous72246306
5157011986157011987GA23GENIChomozygous72246310
5157012258157012259TC22GENIChomozygous72246314
5157013421157013422GA16GENIChomozygous72246317
5157013990157013991GC17GENICpossibly homozygous72246321
5157015115157015116CA4GENIChomozygous73605285
5157015120157015121TG6GENICheterozygous73605288
5157015121157015122GA5GENICheterozygous73605291
5157016024157016025TG24GENIChomozygous72246325
5157016329157016330TC22GENIChomozygous72246329
5157017008157017009GA21GENIChomozygous72246333
5157017454157017455AG14GENIChomozygous71175660
5157018585157018586GA26GENICpossibly homozygous72246337
5157019113157019114AG14GENIChomozygous71175676
5157019545157019546AG23GENICpossibly homozygous72246341
5157021880157021881CG20GENIChomozygous71175680
5157022306157022307CT30GENICpossibly homozygous72246343
5157022527157022528CT22GENICpossibly homozygous72246347
5157022575157022576TC13GENIChomozygous71175684
5157023064157023065AG20GENIChomozygous71175688
5157023295157023296AG22GENIChomozygous71175690
5157002350157002351AT25GENICpossibly homozygous72459509
5157019227157019228AG16GENIChomozygous72459517