chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1263812471263812472GA26GENIChomozygous948973809
1263813164263813165CA20GENIChomozygous948973810
1263813314263813315GA24GENIChomozygous948973811
1263813492263813493TA11GENIChomozygous948973812
1263814051263814052CT24GENIChomozygous948973813
1263815744263815745AG25GENIChomozygous948973814
1263817743263817744AG12GENIChomozygous948973815
1263820813263820814AG23GENIChomozygous948973816
1263820861263820862CT19GENIChomozygous948973817
1263821401263821402GA26GENIChomozygous948973818
1263823231263823232GA15GENIChomozygous948973819
1263823243263823244CT16GENIChomozygous948973820
1263823512263823513AG21GENIChomozygous948973821
1263825765263825766GT13GENIChomozygous948973822
1263827331263827332GA17GENIChomozygous948973823
1263828502263828503CA11GENICpossibly homozygous948973824
1263831722263831723CT26GENIChomozygous948973825
1263832115263832116TC21GENIChomozygous948973826
1263832813263832814AG21GENIChomozygous948973827
1263835278263835279CT23GENIChomozygous948973828
1263835926263835927GA21GENIChomozygous948973829
1263837493263837494GA19GENIChomozygous948973830
1263840846263840847CT21GENIChomozygous948973831
1263842282263842283GT18GENIChomozygous948973832
1263843300263843301AT23GENIChomozygous948973833
1263844963263844964AG21GENIChomozygous948973834