chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3123454486123454487AG19GENIChomozygous957610082
3123466525123466526AG21GENIChomozygous957610083
3123468702123468703AG31GENIChomozygous957610084
3123476583123476584AT19GENIChomozygous957610085
3123476589123476590AT22GENIChomozygous957610086
3123476592123476593CT22GENIChomozygous957610087
3123476598123476599GT22GENIChomozygous957610088
3123476606123476607GT21GENIChomozygous957610089
3123476609123476610CA21GENIChomozygous957610090
3123476623123476624GA22GENIChomozygous957610091
3123476627123476628GC23GENIChomozygous957610092
3123476632123476633TA24GENIChomozygous957610093
3123476680123476681CG32GENIChomozygous957610094
3123476690123476691GA29GENIChomozygous957610095
3123476718123476719TG31GENIChomozygous957610096
3123476726123476727TG29GENIChomozygous957610097
3123493789123493790GA18GENIChomozygous957610098
3123494469123494470AC24GENIChomozygous957610099
3123504390123504391AG23GENIChomozygous957610100
3123507546123507547CG19GENIChomozygous957610101
3123508327123508328GC33GENIChomozygous957610102
3123512363123512364CA32GENIChomozygous957610103
3123514916123514917CT12GENIChomozygous957610104
3123547831123547832TG20GENIChomozygous957610105
3123550770123550771TA11GENIChomozygous957610106
3123551045123551046CT20GENIChomozygous957610107
3123561603123561604GC14GENIChomozygous957610108