chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
25850995258509953CA52GENICpossibly homozygous778969321
25851033758510338AT58GENICpossibly homozygous778969322
25851035758510358TC67GENIChomozygous778969323
25851092158510922CG59GENIChomozygous778969324
25851181958511820AC63GENIChomozygous778969325
25851263358512634GA77GENIChomozygous778969326
25851479858514799GA51GENIChomozygous778969327
25851568258515683CT44GENICpossibly homozygous778969328
25851894158518942GA70GENIChomozygous778969329
25851976458519765TC38GENICpossibly homozygous778969330
25851984858519849TA48GENIChomozygous778969331
25852005158520052CT59GENIChomozygous778969332
25852071858520719CT42GENIChomozygous778969333
25852278258522783GA69GENIChomozygous778969334
25852293458522935CT51GENIChomozygous778969335
25852305158523052TC63GENIChomozygous778969336
25852654058526541CT57GENIChomozygous778969337
25853184058531841TC72GENIChomozygous778969338
25853188358531884TC57GENIChomozygous778969339
25853326758533268GA51GENIChomozygous778969340