chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
74615158546151586AG17GENIChomozygous138083662
74615174846151749TC27GENIChomozygous138083663
74615475146154752AG29GENIChomozygous144030330
74615478446154785TC26GENIChomozygous144030331
74615850946158510GA37GENIChomozygous144030332
74615965146159652AG22GENIChomozygous138083666
74616050046160501GA32GENIChomozygous144030333
74616235146162352TC24GENIChomozygous144030334
74616259946162600GA27GENIChomozygous144030335
74616560746165608GT31GENIChomozygous144030336
74616797746167978GA36GENIChomozygous144030337
74617047046170471AC26GENIChomozygous144030338
74617373646173737GA26GENIChomozygous138083669
74617555946175560CT27GENIChomozygous144030339
74617565446175655AG25GENIChomozygous144030340
74617646646176467CT21GENIChomozygous144030341
74617699146176992CG12GENIChomozygous138083670
74617751446177515CT17GENIChomozygous138083673
74617822146178222TC18GENIChomozygous144030342
74618018046180181AG26GENIChomozygous138083674
74618224246182243GT17GENIChomozygous144030343
74618268946182690TA26GENIChomozygous138083675
74618617546186176GA18GENIChomozygous138083678
74618624146186242CT19GENIChomozygous138083679
74618625246186253GA19GENIChomozygous138083680
74618638646186387GA22GENIChomozygous138083681
74618643346186434TA24GENIChomozygous138083682
74616286446162864AT29GENIChomozygous144005328
74616586046165864AAAT21GENIChomozygous144005329
74618160146181602T22GENIChomozygous144005330
74617746846177469C17GENIChomozygous137951803
74617758946177589ACACATACACATACAT17GENIChomozygous137951804
74618757846187579CA27GENIChomozygous138083684
74618885746188858GA15GENIChomozygous144030344
74618963246189633AG25GENIChomozygous138083687
74619129546191296GA17GENIChomozygous144030345
74617746846177469CA17GENICheterozygous403210131