chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1263812471263812472GA32GENIChomozygous978058893
1263813164263813165CA21GENIChomozygous978058894
1263813314263813315GA36GENICpossibly homozygous978058895
1263813492263813493TA62GENIChomozygous978058896
1263814051263814052CT25GENIChomozygous978058897
1263815744263815745AG37GENIChomozygous978058898
1263817743263817744AG53GENIChomozygous978058899
1263820813263820814AG27GENIChomozygous978058900
1263820861263820862CT29GENIChomozygous978058901
1263821401263821402GA24GENIChomozygous978058902
1263823231263823232GA28GENIChomozygous978058903
1263823243263823244CT28GENIChomozygous978058904
1263823512263823513AG20GENIChomozygous978058905
1263825765263825766GT25GENIChomozygous978058906
1263827331263827332GA25GENIChomozygous978058907
1263828502263828503CA38GENIChomozygous978058908
1263831722263831723CT21GENIChomozygous978058909
1263832115263832116TC21GENIChomozygous978058910
1263832813263832814AG18GENIChomozygous978058911
1263835278263835279CT21GENIChomozygous978058912
1263835926263835927GA10GENIChomozygous978058913
1263837493263837494GA41GENIChomozygous978058914
1263840846263840847CT13GENIChomozygous978058915
1263842282263842283GT39GENIChomozygous978058916
1263843300263843301AT30GENIChomozygous978058917
1263844963263844964AG27GENIChomozygous978058918