chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1263812471263812472GA19GENIChomozygous987109801
1263813164263813165CA19GENIChomozygous987109802
1263813314263813315GA18GENIChomozygous987109803
1263813492263813493TA32GENIChomozygous987109804
1263814051263814052CT34GENIChomozygous987109805
1263815744263815745AG22GENIChomozygous987109806
1263817743263817744AG42GENIChomozygous987109807
1263820813263820814AG16GENIChomozygous987109808
1263820861263820862CT15GENIChomozygous987109809
1263821401263821402GA25GENIChomozygous987109810
1263823231263823232GA21GENIChomozygous987109811
1263823243263823244CT20GENIChomozygous987109812
1263823512263823513AG20GENIChomozygous987109813
1263825226263825227CT6GENIChomozygous987109814
1263825765263825766GT10GENIChomozygous987109815
1263827331263827332GA27GENIChomozygous987109816
1263828502263828503CA22GENIChomozygous987109817
1263831722263831723CT19GENIChomozygous987109818
1263832115263832116TC16GENIChomozygous987109819
1263832813263832814AG20GENIChomozygous987109820
1263834478263834479TC13GENIChomozygous987109821
1263835278263835279CT28GENIChomozygous987109822
1263835926263835927GA11GENIChomozygous987109823
1263837493263837494GA38GENIChomozygous987109824
1263840846263840847CT10GENIChomozygous987109825
1263842282263842283GT34GENIChomozygous987109826
1263843300263843301AT24GENIChomozygous987109827