chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1102478819102478820TG20GENIChomozygous61486428
1102479441102479442CCT16GENICpossibly homozygous61486429
1102479545102479546GA25GENIChomozygous61486430
1102479695102479696TC17GENIChomozygous61486431
1102481516102481517AG26GENIChomozygous61486432
1102481635102481636AAC9GENICpossibly homozygous61486433
1102481778102481779AG24GENIChomozygous61486434
1102482264102482268GGAG----9GENIChomozygous61486435
1102482414102482415CT29GENIChomozygous61486436
1102482542102482543TTC23GENIChomozygous61486437
1102482654102482655GA28GENIChomozygous61486438