chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85890595658905956TT17GENIChomozygous141015623
85890603658906037GC22GENIChomozygous141026739
85890650158906501TGCTGGGC19GENIChomozygous141015624
85890661458906615AG18GENIChomozygous141026740
85890680058906801CT11GENIChomozygous141026741
85890767658907677CT30GENIChomozygous141026743
85890899558908996AG26GENIChomozygous141026744
85890902958909030TC26GENIChomozygous141026745
85890923058909231GA14GENIChomozygous141026746
85890936158909362CT18GENIChomozygous141026747
85890950258909503GA25GENIChomozygous141026748
85891001558910016GC21GENIChomozygous141026749
85891090158910901AGTCGGATCAGAG30GENIChomozygous141015625
85891101258911013GA30GENIChomozygous141026750
85891128258911288TGCTCT17GENIChomozygous141015626
85891177658911777CG32GENIChomozygous141026751
85891178358911784CT30GENIChomozygous141026752
85891270158912702AG22GENIChomozygous141026753
85891291858912919GA26GENIChomozygous141026754
85891298858912990GG24GENIChomozygous141015627
85891326358913266ACT8GENIChomozygous141015628
85891326858913271AAG8GENIChomozygous141015629
85891417658914177AG19GENIChomozygous141026755
85891449158914492CT25GENIChomozygous141026756