chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1141439321141439322GA21GENICpossibly homozygous109327570
1141439743141439744AG20GENIChomozygous108936828
1141439881141439882GA9GENIChomozygous108936829
1141440026141440027TC8GENIChomozygous108936830
1141440771141440772CT13GENIChomozygous108936831
1141440963141440964CT18GENIChomozygous108936832
1141441083141441084AG6GENIChomozygous108936833
1141441834141441835TC14GENIChomozygous108936835
1141441858141441859TA10GENIChomozygous108936836
1141444612141444613CT26GENIChomozygous108936839
1141444667141444668GA25GENIChomozygous108936840
1141445107141445108AG16GENIChomozygous108936841
1141447513141447514CT22GENIChomozygous108936843
1141447726141447727CT30GENIChomozygous108936844
1141447906141447907AG22GENIChomozygous108936845
1141447997141447998GA8GENIChomozygous108936846
1141448002141448003TG12GENIChomozygous108936847
1141448281141448282TC12GENIChomozygous108936849
1141449015141449016GA10GENIChomozygous108936850
1141449575141449576CT17GENIChomozygous108936851
1141449657141449658GT7GENIChomozygous108936852
1141449659141449660GT6GENIChomozygous108936853
1141449674141449675CA9GENIChomozygous108936854
1141450278141450279AT10GENIChomozygous109327572
1141451983141451984GT29GENIChomozygous108260671
1141449714141449715TG4GENIChomozygous125463801
1141448716141448717AC13GENIChomozygous125369076