chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3125175833125175834TC15GENIChomozygous981817389
3125177947125177948AG6GENIChomozygous981817390
3125178018125178019GA17GENIChomozygous981817391
3125178727125178728TC12GENIChomozygous981817392
3125182814125182815TC16GENIChomozygous981817393
3125183305125183306CA16GENIChomozygous981817394
3125186379125186380CT8GENIChomozygous981817395
3125188075125188076GT22GENIChomozygous981817396
3125189281125189282AT22GENIChomozygous981817397
3125189784125189785CT9GENIChomozygous981817398
3125190579125190580CT21GENIChomozygous981817399
3125191474125191475GA21GENIChomozygous981817400
3125199624125199625TC26GENIChomozygous981817401
3125201646125201647CT36GENICpossibly homozygous981817402
3125207139125207140GA27GENIChomozygous981817403
3125207297125207298AG22GENIChomozygous981817404
3125208240125208241GA10GENIChomozygous981817405
3125208438125208439AT4GENIChomozygous981817406
3125208439125208440AT3GENIChomozygous981817407
3125209924125209925AG7GENIChomozygous981817408
3125210006125210007GA13GENIChomozygous981817409
3125210208125210209TC27GENIChomozygous981817410
3125211110125211111GA27GENIChomozygous981817411
3125211485125211486AC16GENICheterozygous981817412
3125212882125212883GA16GENIChomozygous981817413