chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1229442989229442991AA--17GENICpossibly homozygous691860777
1229442990229442991A-17GENICheterozygous691860778
1229446034229446035GGAGGA28GENIChomozygous691860779
1229446053229446054GGAAGC35GENICheterozygous691860780
1229446264229446268AAAA----5GENICheterozygous691860781
1229446519229446520TTGTGC23GENIChomozygous691860783
1229448989229448990GC30GENICheterozygous528050491
1229448989229448990GGCAGAGCGGGATC29GENIChomozygous691860784
1229449934229449935T-33GENIChomozygous691860785
1229450207229450208GC9GENIChomozygous525021224
1229450406229450407CT16GENIChomozygous528050492