chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1229061235229061236AG9GENIChomozygous125469438
1229061996229061997TG21GENIChomozygous125469439
1229062133229062134TA21GENIChomozygous125469440
1229062530229062531TC14GENIChomozygous125469441
1229062837229062838AC8GENIChomozygous125469442
1229063092229063093GA26GENIChomozygous125469443
1229063400229063401CT18GENIChomozygous125469444
1229064819229064820TC15GENIChomozygous125469445
1229065735229065736GA21GENIChomozygous125469446
1229067134229067135CG25GENIChomozygous125469447
1229067982229067983CG4GENIChomozygous125469448
1229069290229069291TA6GENIChomozygous125469449
1229069387229069388AC10GENIChomozygous125469450
1229069571229069572AG12GENICheterozygous125341213
1229069595229069596CA15GENICheterozygous125313708
1229070627229070628CT9GENIChomozygous125469451
1229070850229070851TG20GENIChomozygous125469452
1229071045229071046TA4GENIChomozygous125469453
1229072243229072244TC5GENIChomozygous125469454
1229072343229072344TC15GENIChomozygous125469455
1229073022229073023TC13GENIChomozygous125469456
1229073633229073634AC13GENIChomozygous125313710
1229075187229075188AG14GENIChomozygous125469457
1229075237229075238TC7GENIChomozygous125469458
1229075667229075668TC7GENIChomozygous125469459
1229076352229076353CT26GENIChomozygous125469460
1229076633229076634AC3GENICheterozygous108560698
1229076760229076761CT18GENIChomozygous125469461
1229077507229077508AC21GENIChomozygous125469462
1229077568229077569GT14GENIChomozygous125469463
1229077571229077572AG13GENIChomozygous125469464
1229077719229077720TG13GENIChomozygous109003017
1229078598229078599AG17GENIChomozygous125469465
1229079660229079661TG15GENIChomozygous125469466