chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46284511062845111GA11GENIChomozygous931901573
46284520362845204TC10GENIChomozygous931901574
46284632862846329TC19GENIChomozygous931901575
46284645262846453TC10GENIChomozygous931901576
46284713962847140CG6GENIChomozygous931901577
46284812462848125TG12GENIChomozygous931901578
46284858362848584TC10GENIChomozygous931901579
46284869962848700CT14GENIChomozygous931901580
46285100362851004TC8GENIChomozygous931901581
46285133962851340CT10GENIChomozygous931901582
46285195562851956CT15GENIChomozygous931901583
46285352662853527GA5GENIChomozygous931901584
46285365562853656GT10GENIChomozygous931901585
46285365662853657TC10GENIChomozygous931901586
46285564162855642TC14GENIChomozygous931901587
46285584662855847CT16GENIChomozygous931901588
46285610262856103AG11GENIChomozygous931901589
46285629962856300CT8GENIChomozygous931901590
46285641062856411AC12GENIChomozygous931901591
46285641262856413AG12GENIChomozygous931901592
46285642262856423CT16GENIChomozygous931901593
46285643362856434CT15GENIChomozygous931901594
46285643462856435AG14GENIChomozygous931901595
46285674262856743GA10GENIChomozygous931901596
46285712262857123CT11GENIChomozygous931901597
46285719562857196CT10GENIChomozygous931901598
46285866962858670CT16GENIChomozygous931901599