chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1264094064264094065AG23GENIChomozygous963026020
1264094170264094171GT20GENIChomozygous963026021
1264094261264094262TC22GENIChomozygous963026022
1264094954264094955GA16GENIChomozygous963026023
1264095002264095003TC21GENIChomozygous963026024
1264095870264095871CT28GENIChomozygous963026025
1264095886264095887AG23GENIChomozygous963026026
1264096067264096068CG20GENIChomozygous963026027
1264096228264096229CA22GENIChomozygous963026028
1264096229264096230AT22GENIChomozygous963026029
1264096802264096803GA25GENIChomozygous963026030
1264096893264096894CA29GENIChomozygous963026031
1264096989264096990AG29GENIChomozygous963026032
1264097432264097433TC21GENIChomozygous963026033
1264097484264097485TC28GENIChomozygous963026034
1264097567264097568GA22GENIChomozygous963026035
1264097573264097574GC25GENIChomozygous963026036
1264097633264097634AC36GENIChomozygous963026037
1264097768264097769AG37GENIChomozygous963026038
1264097829264097830TC33GENIChomozygous963026039
1264097923264097924AT32GENIChomozygous963026040
1264098124264098125TC38GENIChomozygous963026041
1264098178264098179GA39GENIChomozygous963026042
1264098215264098216TC39GENIChomozygous963026043
1264099322264099323TC33GENIChomozygous963026044
1264099343264099344AC32GENIChomozygous963026045
1264099366264099367GA26GENIChomozygous963026046
1264099541264099542GA14GENIChomozygous963026047
1264100050264100051GC21GENIChomozygous963026048
1264100637264100638TC36GENIChomozygous963026049
1264100900264100901TG31GENIChomozygous963026050
1264103344264103345CT27GENIChomozygous963026051