chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X154118293154118294CG17GENIChomozygous45322394
X154118348154118349TC17GENIChomozygous45322395
X154119262154119270GGCAGCAG--------9GENIChomozygous45249337
X154121017154121018CT18GENIChomozygous45249338
X154122801154122802CA15GENIChomozygous45322397
X154122988154122989CA9GENIChomozygous45322398
X154124638154124639CCT11GENIChomozygous45322399
X154126322154126323AG17GENIChomozygous45322400
X154127381154127382GA12GENIChomozygous45322401
X154128454154128457AGA---10GENIChomozygous45249342
X154128464154128465GC17GENIChomozygous45798249
X154128959154128960TTTTGTTG7GENIChomozygous45773021
X154131251154131252GA21GENIChomozygous45249343
X154131592154131593GA18GENIChomozygous45322403
X154133231154133232A-6GENICheterozygous45249344
X154133394154133395CCT8GENICpossibly homozygous45322404
X154134002154134003GGACAC7GENICpossibly homozygous45699286
X154136517154136518CCTAT4GENIChomozygous45798250
X154139044154139045GA10GENIChomozygous45322405