chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5134197137134197138AT47GENIChomozygous946962544
5134197325134197326GC45GENIChomozygous946962545
5134197335134197336AC46GENIChomozygous946962546
5134199756134199757TG21GENICheterozygous946962547
5134201506134201507GA32GENICheterozygous946962548
5134201843134201844CT40GENICheterozygous946962549
5134201877134201878CG46GENICheterozygous946962550
5134201929134201930CA46GENICheterozygous946962551
5134204395134204396TC74GENICheterozygous946962552
5134205282134205283GA38GENICheterozygous946962553
5134206121134206122TA64GENICheterozygous946962554
5134206131134206132GA62GENICheterozygous946962555
5134206221134206222GA69GENICheterozygous946962556
5134206223134206224AG72GENICheterozygous946962557
5134206258134206259CT61GENICheterozygous946962558
5134206368134206369GA48GENICheterozygous946962559
5134206406134206407TG62GENICheterozygous946962560
5134206419134206420TC59GENICheterozygous946962561
5134206440134206441GT70GENICheterozygous946962562
5134206464134206465TA72GENICheterozygous946962563
5134206466134206467GT71GENICheterozygous946962564
5134206476134206477AG68GENICheterozygous946962565
5134206519134206520AG77GENICheterozygous946962566
5134206615134206616CT73GENICheterozygous946962567
5134206617134206618GT71GENICheterozygous946962568
5134206667134206668CT74GENICheterozygous946962569
5134206707134206708CT70GENICheterozygous946962570
5134206730134206731AT70GENICheterozygous946962571
5134206744134206745AG78GENICheterozygous946962572
5134206769134206770GA77GENICheterozygous946962573
5134206790134206791AG82GENICheterozygous946962574
5134206886134206887CT86GENICheterozygous946962575
5134206887134206888GA83GENICheterozygous946962576