chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1577170597717060T27GENICheterozygous141120993
1577871927787193G14GENIChomozygous139616745
1578011797801180A14GENICheterozygous139616746
1578395927839593CT19GENICheterozygous403371731
1578395927839593C19GENICheterozygous403371732
1578501527850153G24GENICheterozygous403371733
1578501527850153GC24GENICheterozygous403371734
1578871817887182A5GENICheterozygous403371735
1578871817887182AT5GENICheterozygous403371736
1579056927905694AC23GENICheterozygous139616747
1579947527994753C20GENICheterozygous403371737
1579947527994753CT20GENICheterozygous403371738
1580237798023779T36GENICheterozygous141120994
1578354647835464A36GENICheterozygous141045600
1579947537994754CT20GENICheterozygous139659367
1580188598018860GA38GENICpossibly homozygous139659369