chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104560029545600296CT17GENIChomozygous117008474
104560363945603640TG35GENIChomozygous116584033
104560581145605812AC36GENIChomozygous116584043
104560597045605971CT18GENIChomozygous117008475
104560971045609711AG31GENIChomozygous116584073
104561190745611908CT36GENIChomozygous117008476
104561380345613804GA34GENIChomozygous117008477
104561408345614084GA19GENIChomozygous117008478
104561529745615298CT35GENIChomozygous117008479
104561710645617107CT35GENIChomozygous117008480
104561756645617567GA37GENIChomozygous117008481
104561830945618310GA13GENIChomozygous117008482
104561879945618800GA19GENIChomozygous117008483
104561975745619758AG26GENIChomozygous116584091
104562102145621022AT26GENIChomozygous117008485
104562015645620157AC40GENIChomozygous117008484
104562105545621056AG27GENIChomozygous116771850
104562118445621185GC35GENIChomozygous117008486
104562188145621882TC19GENIChomozygous116771852
104562374945623750AT19GENIChomozygous116584093
104562569245625693TC40GENIChomozygous116584095
104562686045626861TC27GENIChomozygous116771854
104562775045627751CT23GENIChomozygous117008487
104562824645628247CT30GENIChomozygous117008488
104562916945629170GA25GENIChomozygous116930862
104562971145629712CT28GENIChomozygous116771858
104563002345630024AT36GENIChomozygous117008489
104563064745630648CT16GENIChomozygous117008490
104563127145631272AG21GENIChomozygous116930866
104563151245631513GA25GENIChomozygous117008491
104563245445632455GA25GENIChomozygous117008492
104563253445632535TC25GENIChomozygous116930872
104563279345632794AG28GENIChomozygous116930874
104563345845633459AG27GENIChomozygous117008493
104563364645633647GA36GENIChomozygous117008494
104563537845635379GA23GENIChomozygous117008495
104563538045635381TC24GENIChomozygous116584099
104564196945641970AG19GENIChomozygous116584103
104564269145642692CT26GENIChomozygous117008496
104564285645642857GA11GENIChomozygous116584105
104564298445642985AG8GENIChomozygous116584107