chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1229755939229755940AG18GENIChomozygous108561785
1229756034229756035TA17GENIChomozygous108561787
1229756519229756520AC24GENIChomozygous109003366
1229756950229756951TC17GENIChomozygous109003367
1229757490229757491TC13GENIChomozygous109003368
1229757676229757677AG8GENIChomozygous108561799
1229757741229757742AC7GENIChomozygous108561800
1229759255229759256GT13GENIChomozygous109003369
1229759303229759304TC15GENIChomozygous109057219
1229759328229759329GT14GENIChomozygous109003370
1229759482229759483AC21GENICpossibly homozygous109003371
1229759811229759812TA34GENICpossibly homozygous109003372
1229760462229760463TG15GENIChomozygous108561811
1229760489229760490TC14GENIChomozygous109003373
1229760735229760736CA24GENIChomozygous109003374
1229761507229761508TA14GENIChomozygous108561818
1229761719229761720AC8GENIChomozygous108561821
1229762632229762633AG10GENIChomozygous109003375
1229763086229763087CT16GENIChomozygous109003376
1229763456229763457AT8GENIChomozygous108561834
1229763481229763482GA9GENIChomozygous108561836
1229764318229764319CT20GENIChomozygous108561838