chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141761702817617029CA17GENIChomozygous786823515
141762106317621064TC23GENIChomozygous786823516
141762138217621383TC37GENIChomozygous786823517
141762256517622566TA27GENIChomozygous786823518
141762303117623032CT18GENIChomozygous786823519
141762436417624365CT23GENIChomozygous786823520
141762439017624391TC24GENIChomozygous786823521
141762442617624427CG26GENICpossibly homozygous786823522
141762588517625886AG24GENIChomozygous786823523
141762981017629811AG25GENIChomozygous786823524
141762983717629838TC20GENIChomozygous786823525
141762984117629842TC21GENIChomozygous786823526
141762992517629926AG23GENIChomozygous786823527
141763052217630523TA29GENIChomozygous786823528
141763065017630651TG28GENIChomozygous786823529