chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3167542945167542946TG41GENIChomozygous57773362
3167543560167543561GC42GENIChomozygous57773363
3167544919167544920TG26GENIChomozygous57773364
3167545197167545200AAG---35GENIChomozygous57773365
3167548287167548288TC21GENIChomozygous57773367
3167548414167548428GTGTGTGTGTGTGT--------------6GENICheterozygous57773368
3167548416167548428GTGTGTGTGTGT------------6GENICheterozygous57773369
3167549967167549968GA36GENICheterozygous58048963
3167549981167549982GC38GENICheterozygous57773370
3167550026167550027CT42GENICheterozygous57773371
3167550033167550034AG43GENICheterozygous57773372
3167550036167550037AAT38GENICheterozygous57773373
3167550066167550067GA30GENICheterozygous57773374
3167550125167550126CT24GENICheterozygous57773378
3167550136167550137T-22GENICheterozygous57773379
3167551620167551621TC49GENIChomozygous57773380
3167553085167553086AG35GENIChomozygous57773381
3167553540167553541GGAA14GENIChomozygous57773382
3167553612167553613GA23GENIChomozygous57773383
3167553906167553907TC26GENIChomozygous57773384
3167553970167553976TGTGTG------12GENICheterozygous57773385
3167553972167553976TGTG----12GENICheterozygous57773386
3167555983167555984TC37GENIChomozygous57773387
3167556099167556100AG45GENIChomozygous57773388
3167556375167556376G-40GENIChomozygous57773389
3167557172167557173CG48GENIChomozygous57773390
3167558417167558418AAT5GENIChomozygous57773391
3167558540167558541GGA23GENICpossibly homozygous57773392
3167561951167561952AATTT8GENIChomozygous57773394
3167561964167561965CT19GENICheterozygous58399807