chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3123454486123454487AG22GENIChomozygous954634811
3123466525123466526AG17GENIChomozygous954634812
3123468702123468703AG26GENIChomozygous954634813
3123476583123476584AT21GENIChomozygous954634814
3123476589123476590AT23GENIChomozygous954634815
3123476592123476593CT24GENIChomozygous954634816
3123476598123476599GT25GENIChomozygous954634817
3123476606123476607GT24GENIChomozygous954634818
3123476609123476610CA26GENIChomozygous954634819
3123476623123476624GA24GENIChomozygous954634820
3123476627123476628GC26GENIChomozygous954634821
3123476632123476633TA26GENIChomozygous954634822
3123476680123476681CG25GENIChomozygous954634823
3123476690123476691GA22GENIChomozygous954634824
3123476718123476719TG23GENIChomozygous954634825
3123476726123476727TG23GENIChomozygous954634826
3123493789123493790GA26GENIChomozygous954634827
3123494469123494470AC33GENIChomozygous954634828
3123504390123504391AG32GENIChomozygous954634829
3123507546123507547CG20GENIChomozygous954634830
3123508327123508328GC29GENIChomozygous954634831
3123512363123512364CA27GENIChomozygous954634832
3123514916123514917CT17GENIChomozygous954634833
3123547831123547832TG14GENIChomozygous954634834
3123550770123550771TA6GENIChomozygous954634835
3123551045123551046CT13GENIChomozygous954634836
3123561603123561604GC23GENIChomozygous954634837