chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108631858886318589GA5GENIChomozygous126389138
108631921086319211GA9GENICheterozygous117258368
108632007386320074GT20GENIChomozygous116667432
108632117686321177AG22GENIChomozygous116667434
108632166286321663GA16GENIChomozygous116667436
108632223486322235CT18GENIChomozygous116667438
108632227186322272GA27GENIChomozygous117019287
108632232886322329CT7GENIChomozygous116816115
108632233386322334AG5GENIChomozygous116667440
108632329686323297GA13GENIChomozygous117019288
108632330386323304AG14GENIChomozygous117019289
108632353486323535AT15GENIChomozygous117019290
108632359286323593CT9GENIChomozygous117019292
108632453686324537CT25GENIChomozygous117019293
108632529086325291CT19GENIChomozygous117019294
108632572886325729AG20GENIChomozygous117019295
108632634986326350TG5GENIChomozygous117258370
108632636786326368TC5GENIChomozygous117019296
108632745486327455AG23GENIChomozygous117019297
108632769686327697TG10GENIChomozygous117019298
108632795486327955AG19GENIChomozygous117019299
108633008786330088CA17GENIChomozygous126389140
108633092486330925GA24GENIChomozygous117019303
108633483286334833CT18GENIChomozygous117019308
108633483586334836TC20GENIChomozygous116816129
108633488086334881AG18GENIChomozygous117019309
108633534886335349CT15GENIChomozygous117019310