chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1227033847227033848GA23GENIChomozygous109198443
1227034529227034530TA33GENIChomozygous109198445
1227035059227035060CT19GENIChomozygous109198447
1227035177227035178GA27GENIChomozygous109198449
1227035738227035739CT40GENIChomozygous109198451
1227036775227036776AG31GENIChomozygous108998632
1227038039227038040AG28GENIChomozygous109198453
1227039747227039748TG28GENIChomozygous109198455
1227040925227040926TC24GENIChomozygous108998639
1227041647227041648GA38GENIChomozygous109198457
1227041984227041985CT37GENIChomozygous109198459
1227042651227042652CA26GENIChomozygous109198461
1227042858227042859TC32GENIChomozygous108998640
1227042972227042973CT27GENIChomozygous108998641
1227045692227045693GT16GENIChomozygous109198463
1227046445227046446TC26GENIChomozygous108998644
1227047060227047061TC24GENIChomozygous108998645
1227047841227047842TC19GENIChomozygous108998646
1227048615227048616GA29GENICpossibly homozygous109198465
1227048629227048630CT31GENIChomozygous109198467