chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1102915069102915070TC24GENIChomozygous109115375
1102915949102915950AG25GENIChomozygous109115379
1102916994102916995TA19GENIChomozygous109115381
1102917876102917877GA7GENIChomozygous109115383
1102918313102918314GA21GENIChomozygous109115387
1102920051102920052TG20GENIChomozygous109115389
1102921573102921574CT15GENIChomozygous109115391
1102923364102923365CT16GENIChomozygous109115395
1102923491102923492GA8GENIChomozygous109115397
1102925081102925082CT23GENIChomozygous109115399
1102925086102925087AG22GENIChomozygous109115401
1102925549102925550GA24GENIChomozygous109115403
1102925703102925704TC26GENIChomozygous109115405
1102926657102926658AG21GENIChomozygous109115407
1102926705102926706TC19GENIChomozygous109115409
1102926848102926849TC19GENIChomozygous109115411
1102926877102926878CT18GENIChomozygous109115413
1102927694102927695GA28GENIChomozygous109115419
1102929262102929263GA24GENIChomozygous109115423