chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
204851419048514191AC29GENIChomozygous109276549
204851446648514467CG20GENIChomozygous109213922
204851519848515199AG14GENIChomozygous109348213
204851532748515328AG27GENIChomozygous109213924
204851729148517292GA35GENIChomozygous109405667
204852012548520126TG13GENIChomozygous109405668
204852102048521021CT20GENIChomozygous109405669
204852102148521022TG20GENIChomozygous109405670
204852105648521057CT18GENIChomozygous109405671
204852211848522119TC8GENIChomozygous109276565
204852233348522334AC25GENIChomozygous109276571
204852234648522347CA13GENIChomozygous109276573
204852237548522376GT12GENIChomozygous109276575
204852274148522742AC39GENIChomozygous109213928
204852286948522870CT35GENIChomozygous109213930
204852299148522992CT24GENIChomozygous109213932
204852337448523375TA31GENIChomozygous109405672
204855079448550795TG17GENIChomozygous109405673
204857260148572602TC23GENIChomozygous109405674