chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
112713057127130571GGTTT23GENIChomozygous128893475
112713084227130842A15GENIChomozygous128893476
112713111527131116G15GENICpossibly homozygous128893477
112713646527136465G20GENIChomozygous128893478
112713648727136488TC22GENIChomozygous116033051
112713520827135209AG17GENIChomozygous115799147
112713535427135355AC27GENIChomozygous115799149
112713280627132807AC22GENIChomozygous116033047
112713613127136132CA24GENIChomozygous116033049
112713665727136658GA29GENIChomozygous116033053
112713722227137223AT24GENIChomozygous116033055
112713729327137294AG30GENIChomozygous115799151
112713762527137626GT24GENIChomozygous115799153
112713972527139726AC26GENIChomozygous115799155
112714137127141372CT20GENIChomozygous115799159
112714105427141057AAT18GENIChomozygous131103801