chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
38036411380364114AG23GENIChomozygous112390328
38036743680367437CT5GENIChomozygous125864215
38036744080367441CT5GENIChomozygous125864216
38036796280367963CT15GENIChomozygous112390329
38036741580367416CT8GENIChomozygous125827283
38036742780367428AC7GENIChomozygous125827284
38036748680367487AC9GENIChomozygous125827285
38037190880371909CG25GENIChomozygous111635293
38037462180374622TA16GENIChomozygous112390331
38037904780379048TC14GENIChomozygous112390332
38038053780380538TC13GENICheterozygous111635296
38038982880389829TC14GENIChomozygous111635305
38039073280390733GA19GENIChomozygous112390334
38039478780394788CT19GENIChomozygous111635309
38039905280399053CT16GENIChomozygous112390335
38039957480399575TC13GENIChomozygous111635312
38040131380401314GA20GENIChomozygous112241979
38040182380401824AC19GENICpossibly homozygous112241981
38040338080403381TA19GENIChomozygous111635315
38040381380403814CT22GENIChomozygous112390336
38040392880403929CT12GENIChomozygous111635316
38040438480404385TA17GENIChomozygous112241982
38040642380406424TC9GENIChomozygous111635319
38040956180409562GC8GENIChomozygous125827287
38040957980409580AG13GENIChomozygous125827288
38041178480411785AG23GENIChomozygous111635335