chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2105059558105059559TG13GENIChomozygous110580356
2105061277105061278TC17GENIChomozygous110580358
2105061315105061316CT27GENIChomozygous110580360
2105062485105062486AG16GENIChomozygous110580362
2105063022105063023AT13GENIChomozygous109962102
2105065987105065988CT13GENIChomozygous110580364
2105066277105066278CT13GENIChomozygous110580366
2105067585105067586TC6GENIChomozygous110580368
2105069215105069216GA34GENIChomozygous110580370
2105069524105069525GA16GENIChomozygous110580372
2105069624105069625CA15GENIChomozygous125577689
2105069735105069736TG6GENIChomozygous125577690
2105070730105070731TA13GENIChomozygous110580374
2105072817105072818TA19GENIChomozygous109962118
2105073189105073190TG12GENIChomozygous109962120
2105074259105074260CG15GENIChomozygous110580378
2105074379105074380AT13GENIChomozygous109962122
2105074687105074688CA18GENIChomozygous110580380
2105076146105076147AT16GENIChomozygous109962128
2105078736105078737CA15GENIChomozygous110580382
2105080634105080635GT13GENIChomozygous125577691
2105080635105080636GA14GENIChomozygous125577692
2105080706105080707TG17GENIChomozygous125577693
2105081364105081365GA22GENIChomozygous109962150
2105081640105081641TC16GENIChomozygous109962153
2105082984105082985GA18GENIChomozygous110580386
2105083996105083997AT19GENIChomozygous110580388
2105084829105084830AC19GENIChomozygous109962161
2105085011105085012CT5GENIChomozygous110580390
2105086231105086232GA10GENIChomozygous109962163
2105086240105086241AG8GENIChomozygous109962164
2105086818105086819AC13GENIChomozygous109962170
2105087302105087303GC10GENIChomozygous110580392
2105087578105087579CA12GENIChomozygous109962176
2105088266105088267TC16GENIChomozygous110580396
2105087176105087177GA6GENICheterozygous125649374