chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
74615158546151586AG69GENIChomozygous138083662
74615174846151749TC65GENIChomozygous138083663
74615475146154752AG62GENIChomozygous144030330
74615478446154785TC68GENIChomozygous144030331
74615850946158510GA62GENIChomozygous144030332
74615965146159652AG52GENIChomozygous138083666
74616050046160501GA47GENIChomozygous144030333
74616235146162352TC58GENIChomozygous144030334
74616259946162600GA47GENIChomozygous144030335
74616560746165608GT57GENIChomozygous144030336
74616797746167978GA53GENIChomozygous144030337
74617047046170471AC62GENIChomozygous144030338
74617373646173737GA50GENIChomozygous138083669
74617555946175560CT55GENIChomozygous144030339
74617565446175655AG52GENIChomozygous144030340
74617646646176467CT58GENIChomozygous144030341
74617699146176992CG64GENIChomozygous138083670
74617751446177515CT33GENIChomozygous138083673
74616286446162864AT44GENIChomozygous144005328
74616586046165864AAAT49GENICpossibly homozygous144005329
74617822146178222TC52GENIChomozygous144030342
74618018046180181AG58GENIChomozygous138083674
74618160146181602T58GENIChomozygous144005330
74618224246182243GT53GENIChomozygous144030343
74618268946182690TA43GENIChomozygous138083675
74618617546186176GA63GENIChomozygous138083678
74618624146186242CT67GENIChomozygous138083679
74618625246186253GA66GENIChomozygous138083680
74618638646186387GA71GENIChomozygous138083681
74618643346186434TA63GENIChomozygous138083682
74618757846187579CA65GENIChomozygous138083684
74618885746188858GA51GENIChomozygous144030344
74617758946177589ACACATACACATACAT44GENIChomozygous137951804
74617746846177469CA36GENICheterozygous403210131
74617746846177469C36GENIChomozygous137951803
74618963246189633AG62GENIChomozygous138083687
74619129546191296GA72GENIChomozygous144030345