chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3167542945167542946TG40GENIChomozygous57773362
3167543560167543561GC40GENIChomozygous57773363
3167544919167544920TG37GENIChomozygous57773364
3167545197167545200AAG---27GENIChomozygous57773365
3167548287167548288TC29GENIChomozygous57773367
3167548414167548428GTGTGTGTGTGTGT--------------10GENICheterozygous57773368
3167548416167548428GTGTGTGTGTGT------------10GENICheterozygous57773369
3167549981167549982GC42GENICheterozygous57773370
3167550026167550027CT49GENICheterozygous57773371
3167550033167550034AG47GENICheterozygous57773372
3167550036167550037AAT41GENICheterozygous57773373
3167550066167550067GA29GENICheterozygous57773374
3167550116167550117TA12GENIChomozygous57773375
3167550125167550126CT18GENICheterozygous57773378
3167550136167550137T-19GENICheterozygous57773379
3167551620167551621TC45GENIChomozygous57773380
3167553085167553086AG50GENIChomozygous57773381
3167553540167553541GGAA19GENICpossibly homozygous57773382
3167553612167553613GA23GENIChomozygous57773383
3167553906167553907TC33GENIChomozygous57773384
3167553970167553976TGTGTG------18GENICheterozygous57773385
3167553972167553976TGTG----18GENICheterozygous57773386
3167555983167555984TC42GENIChomozygous57773387
3167556099167556100AG35GENIChomozygous57773388
3167556375167556376G-35GENIChomozygous57773389
3167557172167557173CG36GENIChomozygous57773390
3167558417167558418AAT13GENIChomozygous57773391
3167558540167558541GGA24GENICheterozygous57773392
3167561951167561952AATTT23GENIChomozygous57773394