chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
151398818013988181CG9GENICheterozygous48465162
151401254314012544C-6GENIChomozygous48232683
151401254514012546GGT6GENIChomozygous48232684
151404844214048443TTA7GENIChomozygous48232689
151404846014048461TG7GENIChomozygous48232690
151404846314048464CA6GENIChomozygous48232691
151409410514094106C-7GENIChomozygous48232699
151409412114094122GGA2GENIChomozygous48232700
151411249414112496TT--23GENICpossibly homozygous48232703
151411261814112619GGT15GENIChomozygous48232704
151417204514172046GT1GENIChomozygous48232714
151417204714172048CT1GENIChomozygous48564964
151417204814172049TA1GENIChomozygous48232715
151417206214172063TA1GENIChomozygous48232716
151417206714172068TG4GENIChomozygous48232717
151415856514158587CACACACATGCGCGCGCGCGCG----------------------2GENICheterozygous48944967
151418818614188187AAG4GENIChomozygous48232718
151420313614203137GT10GENICheterozygous48232720
151420668714206688GC12GENICpossibly homozygous48232723
151421667814216679A-10GENIChomozygous48232724
151421669514216696GT14GENIChomozygous48232725
151423531114235312GGCACACA7GENICheterozygous48944969
151426688514266886CCAAA3GENICheterozygous48944971
151428359614283597AT13GENICheterozygous48930528
151428543514285436T-2GENICheterozygous48805502
151428647014286471AAG5GENICheterozygous48944973