chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3167542945167542946TG22GENIChomozygous57773362
3167543560167543561GC25GENIChomozygous57773363
3167544919167544920TG23GENIChomozygous57773364
3167545197167545200AAG---19GENIChomozygous57773365
3167546266167546280GTGGTACTGCAAAG--------------39GENICheterozygous58631353
3167548287167548288TC11GENIChomozygous57773367
3167548416167548428GTGTGTGTGTGT------------17GENIChomozygous57773369
3167550066167550067GA13GENIChomozygous57773374
3167550113167550114CG13GENIChomozygous58048964
3167550115167550117CT--13GENIChomozygous58631354
3167550118167550119AATG13GENIChomozygous58631355
3167550120167550121AG14GENIChomozygous57773377
3167550125167550126CT14GENIChomozygous57773378
3167551620167551621TC35GENIChomozygous57773380
3167553085167553086AG29GENIChomozygous57773381
3167553540167553541GGAA9GENIChomozygous57773382
3167553612167553613GA21GENIChomozygous57773383
3167553906167553907TC32GENIChomozygous57773384
3167553972167553976TGTG----17GENICpossibly homozygous57773386
3167555983167555984TC30GENIChomozygous57773387
3167556099167556100AG21GENIChomozygous57773388
3167556375167556376G-28GENIChomozygous57773389
3167557172167557173CG15GENIChomozygous57773390
3167558540167558541GGA8GENIChomozygous57773392
3167561951167561952AATTT10GENICheterozygous57773394
3167561951167561952AATT10GENICheterozygous57773395