chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1172592294172592295AAT4GENICheterozygous60945603
1172592294172592295AATT4GENICheterozygous60945604
1172592646172592647AG7GENICheterozygous61309984
1172592835172592836CT13GENIChomozygous60945607
1172594780172594781TC26GENIChomozygous60945609
1172594781172594782TC27GENIChomozygous60945610
1172597823172597824TC33GENIChomozygous60945611
1172598621172598622AT24GENIChomozygous61785938
1172599512172599513TC17GENIChomozygous60945613
1172602052172602053TTTTTGTTTG10GENICpossibly homozygous61961413
1172594720172594721TC29GENIChomozygous61961410
1172596748172596749AAC17GENIChomozygous61961411
1172600637172600638TG21GENIChomozygous61961412
1172603707172603708CT40GENIChomozygous61961414