chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1237338673733868AG28GENIChomozygous66599605
1237346943734695CT5GENIChomozygous66599606
1237474143747415CT27GENIChomozygous66599607
1237482093748210CG31GENIChomozygous66599608
1237484233748424CA23GENIChomozygous66599609
1237507333750734AT13GENIChomozygous66599610
1237550523755053CA27GENIChomozygous66599612
1237556953755696CT18GENIChomozygous66599613
1237572513757252GT34GENIChomozygous66599614
1237613023761303AG16GENIChomozygous66599616
1237622863762287AG21GENIChomozygous66599617
1237638713763872AC12GENICheterozygous66599618
1237640993764100GA13GENICheterozygous66599621
1237641063764107CT10GENICheterozygous66599622
1237642553764256TC22GENIChomozygous66599623
1237678983767899GA24GENIChomozygous66599624
1237690383769039GA17GENIChomozygous66599625
1237691343769135GC24GENIChomozygous66599626
1237691843769185CG11GENIChomozygous66599627
1237694533769454CG21GENIChomozygous66599628
1237721883772189AC17GENIChomozygous66599629