chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1190387901190387902GT57GENICheterozygous108465292
1190387923190387924CT60GENICheterozygous108465293
1190387929190387930GA63GENICheterozygous108465294
1190387931190387932CT65GENICheterozygous108465295
1190388265190388266CT33GENICheterozygous108977686
1190388308190388309AG28GENICpossibly homozygous108465297
1190388346190388347AT19GENICheterozygous108465298
1190388386190388387GA29GENICpossibly homozygous108465299
1190388971190388972GT56GENICheterozygous108465308
1190388977190388978CT58GENICheterozygous108465309
1190388983190388984TC56GENICheterozygous108465310
1190388998190388999GA56GENICheterozygous108465311
1190389002190389003CA54GENICheterozygous108465312
1190389005190389006CT53GENICheterozygous108465313
1190389014190389015CA56GENICheterozygous108977689
1190389045190389046GT42GENICheterozygous108465314
1190389046190389047GT42GENICheterozygous108465315
1190389053190389054GA44GENICheterozygous108465316