chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X111230776111230777AC15GENIChomozygous45194221
X111293301111293302TC17GENICheterozygous45949061
X111293336111293337GT19GENICheterozygous45949062
X111293350111293351TG19GENICheterozygous45949063
X111293363111293364GC18GENICheterozygous45949064
X111293369111293370AG18GENICheterozygous45949065
X111293376111293377CT14GENICheterozygous45949066
X111293383111293384CT14GENICheterozygous45949067
X111293384111293385AAC14GENICheterozygous45949068
X111293395111293396TC14GENICheterozygous45949069
X111298049111298050TC10GENIChomozygous45194287
X111298057111298060ACT---10GENIChomozygous45520773
X111298061111298062AG5GENIChomozygous45520775
X111298062111298063AATTT5GENIChomozygous45520777
X111298499111298500TA14GENIChomozygous45194289
X111343508111343509CCA8GENIChomozygous45194343
X111371597111371598AAG10GENIChomozygous45194397
X111371620111371621GGT11GENIChomozygous45194398
X111387244111387245T-15GENIChomozygous45194438
X111387888111387889GGT13GENICheterozygous45696830
X111388045111388046CT13GENICheterozygous45194441
X111388376111388377TC10GENICheterozygous45194444
X111431222111431223TC12GENIChomozygous45311568
X111388005111388006AT11GENICheterozygous45968528