chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1102915069102915070TC16GENIChomozygous109115375
1102915393102915394TC16GENIChomozygous109115377
1102915949102915950AG31GENIChomozygous109115379
1102916994102916995TA13GENIChomozygous109115381
1102917876102917877GA6GENIChomozygous109115383
1102918313102918314GA18GENIChomozygous109115387
1102920051102920052TG16GENIChomozygous109115389
1102922013102922014TC4GENIChomozygous109420107
1102923364102923365CT19GENIChomozygous109115395
1102923491102923492GA17GENIChomozygous109115397
1102925081102925082CT21GENIChomozygous109115399
1102925086102925087AG21GENIChomozygous109115401
1102925549102925550GA21GENIChomozygous109115403
1102925703102925704TC29GENIChomozygous109115405
1102926657102926658AG24GENIChomozygous109115407
1102926705102926706TC20GENIChomozygous109115409
1102926848102926849TC22GENIChomozygous109115411
1102926877102926878CT24GENIChomozygous109115413
1102929262102929263GA24GENIChomozygous109115423