chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108934191189341912AG14GENIChomozygous804103346
108934338689343387AG18GENIChomozygous804103347
108934367489343675CT23GENIChomozygous804103348
108934414389344144AG20GENIChomozygous804103349
108934466889344669GA18GENIChomozygous804103350
108934523189345232GA27GENICpossibly homozygous804103351
108934561589345616GC20GENICpossibly homozygous804103352
108934608789346088AT13GENIChomozygous804103353
108934668089346681CT24GENIChomozygous804103354
108934699089346991TC32GENICpossibly homozygous804103355
108934822789348228AG19GENIChomozygous804103356
108934825989348260CT20GENICpossibly homozygous804103357
108934854189348542GA22GENIChomozygous804103358
108934863289348633GA26GENIChomozygous804103359
108934864889348649CT26GENIChomozygous804103360
108934868889348689TC28GENIChomozygous804103361
108934897189348972AC30GENIChomozygous804103362
108934901089349011GA21GENIChomozygous804103363
108934917489349175TC25GENIChomozygous804103364
108934918689349187CG26GENIChomozygous804103365