chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
63000353030003531GA36GENIChomozygous789783378
63000386330003864AG22GENIChomozygous789783379
63000439130004392AG12GENIChomozygous789783380
63000456730004568TC11GENIChomozygous789783381
63000481430004815GA13GENIChomozygous789783382
63000485630004857CT19GENIChomozygous789783383
63000492230004923GA28GENIChomozygous789783384
63000506430005065TC10GENIChomozygous789783385
63000545030005451AT2GENIChomozygous789783386
63000548530005486CT27GENIChomozygous789783387
63000552830005529AG21GENIChomozygous789783388
63000573930005740TC26GENIChomozygous789783389
63000596030005961GA24GENIChomozygous789783390
63000598030005981TC28GENIChomozygous789783391
63000712430007125CT23GENIChomozygous789783392
63000721330007214AG25GENIChomozygous789783393
63000783330007834GA20GENIChomozygous789783394
63000789830007899TC26GENIChomozygous789783395
63000790630007907TG29GENIChomozygous789783396
63000797230007973CG19GENIChomozygous789783397
63000800330008004AG28GENIChomozygous789783398
63000825330008254TC17GENIChomozygous789783399
63000874430008745CA14GENIChomozygous789783400
63000874630008747TA14GENIChomozygous789783401
63000882830008829TG17GENIChomozygous789783402
63000901730009018GA13GENIChomozygous789783403
63000902030009021CT12GENIChomozygous789783404
63000904930009050TC17GENIChomozygous789783405
63000924130009242TC18GENIChomozygous789783406
63000946330009464TA8GENICpossibly homozygous789783407
63000946730009468CT9GENIChomozygous789783408
63000948130009482TA13GENIChomozygous789783409