chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1263812471263812472GA22GENIChomozygous810782896
1263813164263813165CA20GENIChomozygous810782897
1263813314263813315GA19GENIChomozygous810782898
1263813492263813493TA32GENIChomozygous810782899
1263814051263814052CT34GENIChomozygous810782900
1263815349263815350GA31GENICpossibly homozygous810782901
1263815744263815745AG23GENIChomozygous810782902
1263817743263817744AG44GENIChomozygous810782903
1263820813263820814AG16GENIChomozygous810782904
1263820861263820862CT17GENIChomozygous810782905
1263821401263821402GA26GENIChomozygous810782906
1263823231263823232GA23GENIChomozygous810782907
1263823243263823244CT22GENIChomozygous810782908
1263823512263823513AG21GENIChomozygous810782909
1263825226263825227CT26GENICheterozygous810782910
1263825765263825766GT10GENIChomozygous810782911
1263827331263827332GA27GENIChomozygous810782912
1263828502263828503CA23GENIChomozygous810782913
1263831722263831723CT22GENIChomozygous810782914
1263832115263832116TC16GENIChomozygous810782915
1263832813263832814AG20GENIChomozygous810782916
1263835278263835279CT28GENIChomozygous810782917
1263835926263835927GA11GENIChomozygous810782918
1263837493263837494GA40GENIChomozygous810782919
1263840846263840847CT11GENIChomozygous810782920
1263842282263842283GT34GENIChomozygous810782921
1263843300263843301AT25GENIChomozygous810782922
1263844963263844964AG29GENICpossibly homozygous810782923