chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1251510704251510705TA15GENIChomozygous622870783
1251511792251511798TTGTTG------3GENIChomozygous740078575
1251513192251513193TC23GENICpossibly homozygous622870784
1251514666251514667TC17GENIChomozygous622870785
1251519595251519597AT--16GENICpossibly homozygous740078576
1251519619251519620AG13GENIChomozygous622870786
1251520164251520165TG14GENIChomozygous622870787
1251520451251520452TG17GENICpossibly homozygous622870788
1251521715251521716CT13GENICpossibly homozygous622870789
1251522038251522039A-6GENICheterozygous740078577
1251522075251522076CG7GENIChomozygous622870790
1251523341251523342C-10GENIChomozygous740078578
1251523343251523344GT11GENIChomozygous622870791
1251524211251524212CG14GENIChomozygous622870792