chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121893135918931360GA4GENICheterozygous890363387
121893170118931702GC10GENIChomozygous890363386
121893184418931845GA6GENIChomozygous890363385
121893185618931857CT7GENIChomozygous890363384
121893194618931947AG10GENIChomozygous890363383
121893227018932271TC20GENIChomozygous890363382
121893231118932312CT20GENIChomozygous890363381
121893313018933131AG14GENIChomozygous890363380
121893470118934702AG7GENIChomozygous890363379
121893489518934896GA8GENIChomozygous890363378
121893571718935718TA17GENIChomozygous890363377
121893631918936320AG15GENIChomozygous890363376
121893694918936950GA12GENIChomozygous890363375
121893759218937593CT6GENIChomozygous890363374