chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18812230188122302AG32GENIChomozygous74217083
18812317788123178GA49GENIChomozygous74217086
18812340288123403TC37GENIChomozygous74217089
18812379088123791TC26GENIChomozygous74217091
18812412788124128TC39GENIChomozygous74217094
18812432588124326GA61GENIChomozygous74217097
18812749488127495GC27GENIChomozygous75058837
18812763088127631AT53GENIChomozygous75058841
18812783388127834GA18GENIChomozygous75058851
18812801988128020GC28GENIChomozygous75058861
18812340388123404CT38GENIChomozygous75426381
18812420888124209GA28GENIChomozygous75689367
18812609988126100GA20GENIChomozygous75689369
18812641588126416AT18GENIChomozygous75689371
18812674788126748AG44GENIChomozygous75689373
18812691988126920TC51GENIChomozygous75689375
18812750288127503TA26GENIChomozygous75689377
18812557288125573AG9GENIChomozygous76524823
18812558188125582TC9GENIChomozygous76632227
18812559988125600GA6GENICheterozygous78298192
18812850388128504CA17GENIChomozygous75689379
18812860488128605GA36GENIChomozygous74217109
18812903988129040GA27GENIChomozygous75689381
18812916088129161GA28GENIChomozygous75058873
18812949688129497CA36GENIChomozygous75058875
18812950688129507TG46GENIChomozygous75058877
18812951788129518GC59GENIChomozygous75689383
18812982888129829AG38GENIChomozygous75058879