chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3143096579143096580TG40GENIChomozygous112172385
3143096713143096714TC25GENICheterozygous112256808
3143096860143096861GC56GENICpossibly homozygous112172389
3143097410143097411GA29GENIChomozygous112172391
3143097423143097424TC33GENIChomozygous112172393
3143098097143098098GT55GENIChomozygous112172395
3143098123143098124AG47GENIChomozygous112172397
3143098654143098655GA32GENICpossibly homozygous112172399