chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1461742416174242GA2GENIChomozygous1001510546
1461743086174309CT4GENIChomozygous1001510547
1461746646174665AC8GENIChomozygous1001510548
1461747076174708AG8GENIChomozygous1001510549
1461750996175100GC7GENIChomozygous1001510550
1461758556175856TC2GENIChomozygous1001510551
1461762496176250TC3GENIChomozygous1001510552
1461767686176769AT5GENIChomozygous1001510553
1461771496177150TC5GENIChomozygous1001510554
1461774006177401GC3GENIChomozygous1001510555
1461774566177457TC5GENIChomozygous1001510556
1461775596177560AG8GENIChomozygous1001510557
1461776266177627AG3GENIChomozygous1001510558
1461778906177891TA5GENIChomozygous1001510559
1461811396181140GA6GENIChomozygous1001510560
1461997406199741TA5GENIChomozygous1001510561
1462170706217071GA5GENIChomozygous1001510562
1462170726217073GC5GENIChomozygous1001510563
1462170766217077GC5GENIChomozygous1001510564
1462170806217081GC5GENIChomozygous1001510565
1462173686217369CT4GENIChomozygous1001510566
1462177876217788TA8GENIChomozygous1001510567
1462178456217846CT8GENIChomozygous1001510568
1462179876217988CT6GENIChomozygous1001510569
1462182606218261AG5GENIChomozygous1001510570
1462188826218883CG5GENIChomozygous1001510571
1462191226219123CT3GENIChomozygous1001510572
1462193136219314CT4GENIChomozygous1001510573
1462202146220215CG4GENIChomozygous1001510574
1462207146220715AG10GENIChomozygous1001510575