chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1237338673733868AG33GENIChomozygous66599605
1237346943734695CT8GENICpossibly homozygous66599606
1237474143747415CT18GENIChomozygous66599607
1237482093748210CG24GENIChomozygous66599608
1237484233748424CA23GENIChomozygous66599609
1237507333750734AT11GENIChomozygous66599610
1237550523755053CA20GENIChomozygous66599612
1237556953755696CT20GENIChomozygous66599613
1237572513757252GT28GENIChomozygous66599614
1237613023761303AG36GENIChomozygous66599616
1237622863762287AG14GENIChomozygous66599617
1237638713763872AC18GENIChomozygous66599618
1237640993764100GA14GENICheterozygous66599621
1237641063764107CT14GENICpossibly homozygous66599622
1237642553764256TC22GENIChomozygous66599623
1237678983767899GA26GENIChomozygous66599624
1237690383769039GA23GENIChomozygous66599625
1237691343769135GC28GENIChomozygous66599626
1237691843769185CG19GENIChomozygous66599627
1237694533769454CG20GENIChomozygous66599628
1237721883772189AC4GENIChomozygous66599629