chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106157176061571761TA19GENIChomozygous138802370
106157498861574989CT16GENIChomozygous144867342
106157505961575060AG13GENIChomozygous145149046
106157506161575062AG13GENIChomozygous145149047
106157507561575076GA13GENIChomozygous145149048
106157519861575200CA7GENIChomozygous144855958
106157529761575298TC18GENIChomozygous138802372
106157614461576145TC24GENIChomozygous138802373
106157887561578876A20GENIChomozygous138686683
106157511261575120CACACACG12GENIChomozygous145148371
106157643361576434A14GENICpossibly homozygous138686682
106157899661578997AT28GENIChomozygous144867343
106157925661579257AG23GENIChomozygous138802376
106158011261580122AGAGACTCTA16GENIChomozygous144855959
106158172461581725GA20GENIChomozygous138802382
106158190561581905A20GENIChomozygous144855960
106158323361583239CACACG11GENIChomozygous138686687
106158492561584926GT16GENIChomozygous144867345
106158769361587694TA14GENICheterozygous403288292
106157510461575105T15GENICheterozygous403288286
106157510461575105TC15GENIChomozygous403288287
106157529761575298T18GENICheterozygous403288289
106158769361587694T14GENICheterozygous403288291
106158769761587698T14GENICheterozygous403288296
106158769561587696TA14GENICheterozygous403288293
106158769561587696T14GENICheterozygous403288294
106158769761587698TA14GENICheterozygous403288295
106158888061588881AG20GENIChomozygous138802385
106158899861588999GA17GENIChomozygous144867346
106159149361591494CT7GENIChomozygous154658097
106159149361591494CA7GENICheterozygous403288299
106159149361591494C7GENICheterozygous403288300
106159323261593233CT17GENICpossibly homozygous144867347
106159328061593281TC14GENICpossibly homozygous138802389
106160715261607153CT17GENIChomozygous144867351
106160226161602262CT14GENIChomozygous144867350
106160403861604039TA17GENIChomozygous138802394
106160559561605596AT14GENIChomozygous138802396