chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6115096625115096626AG49GENICheterozygous927164638
6115096914115096915CT49GENICheterozygous927164639
6115097145115097146GGC31GENICheterozygous927226263
6115097198115097199GA37GENICheterozygous927164640
6115097225115097226GGCAGATGCA39GENICheterozygous927226264
6115098265115098266CCA29GENICheterozygous927226265
6115098266115098267TG27GENICheterozygous927164641
6115098409115098410AC12GENICheterozygous927164642
6115114950115114951TG14GENICheterozygous927164643
6115140806115140807CT21GENICheterozygous927164644
6115140813115140814AT23GENICheterozygous927164645
6115142420115142421GT19GENICheterozygous927164646
6115142747115142748CT22GENICheterozygous927164647
6115142764115142765CT28GENICheterozygous927164648
6115149947115149948GA14GENICheterozygous927164649
6115150146115150147CT14GENICheterozygous927164650