chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
79962624799626248AG20GENIChomozygous116217672
79962781099627811AG30GENIChomozygous116217673
79962932399629324CG35GENICpossibly homozygous116217674
79963048599630486AC34GENIChomozygous116217675
79963077699630777GA36GENIChomozygous116217676
79963276699632767CT44GENIChomozygous116217677
79963354999633550CG22GENIChomozygous116217678
79963494799634948TC35GENIChomozygous116217679
79963561799635618CT18GENIChomozygous116217680
79963574199635742CG29GENIChomozygous116217681
79963580699635807TC23GENIChomozygous116217682
79963718599637186CT19GENIChomozygous116217683
79963911199639112TC25GENIChomozygous115785892
79963932799639328AG27GENIChomozygous116217684
79963952299639523CG24GENIChomozygous116217685
79964076699640767GA30GENIChomozygous116217690
79964114399641144CA32GENIChomozygous116217691
79964581299645813AT21GENIChomozygous116217692
79965331599653316AG49GENIChomozygous116217693
79965423399654234GA27GENIChomozygous115785894
79965448599654486CT31GENIChomozygous115785900
79965822799658228CT43GENIChomozygous116217698
79965867699658677CT33GENIChomozygous116217699
79966048999660490CA32GENIChomozygous116217700
79966080899660809CG23GENIChomozygous116217701
79966377299663773AG28GENIChomozygous116217702
79966778099667781GA22GENIChomozygous116217703
79966784799667848TC23GENIChomozygous116217704
79967021699670217AC24GENIChomozygous116217705
79967147199671472TC23GENIChomozygous116217706
79967227699672277CT24GENIChomozygous116217707
79967241699672417GA28GENIChomozygous116217708
79967301499673015CT27GENIChomozygous116217709
79967552999675530AT34GENIChomozygous116217712
79967648799676488TC25GENIChomozygous116217713