chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
17323081173230812GA38GENIChomozygous109415082
17323354573233546AG28GENIChomozygous109415083
17323889873238899CT15GENICheterozygous109107471
17323859473238595AT24GENIChomozygous108133432
17323257773232577T36GENICpossibly homozygous131777686
17323895673238957CA29GENICheterozygous121258020
17324052973240530AG31GENICpossibly homozygous108867038
17324158973241590GA38GENICheterozygous108867041
17324197773241978TC28GENICpossibly homozygous109497308
17324320873243209TC25GENIChomozygous108867049
17324476773244768GT32GENIChomozygous109415085
17324621673246217TC30GENIChomozygous108867054
17325020673250206A29GENIChomozygous131777687
17325137073251371AT33GENIChomozygous109415086
17325508573255086TA24GENIChomozygous108867060
17325624573256246TC5GENIChomozygous125427053
17324503273245032AGATGAAATGAAACCTGAAGAG7GENIChomozygous130619178
17325041773250417A26GENIChomozygous131777688
17326295973262959GT20GENICpossibly homozygous131777689