chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1218122478218122479TA20GENICpossibly homozygous61087041
1218122479218122480TTAC15GENIChomozygous61087042
1218127523218127524TTAC14GENIChomozygous61087047
1218127551218127553CG--25GENICpossibly homozygous61087048
1218127552218127553GA28GENIChomozygous61087049
1218130729218130730CT28GENIChomozygous61592146