chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1170600356170600357CA31GENIChomozygous109166817
1170600843170600844GA22GENIChomozygous109166819
1170601709170601710AT17GENIChomozygous108376219
1170606236170606237AG46GENIChomozygous108376223
1170610794170610795AG31GENIChomozygous108376238
1170615839170615840CT33GENIChomozygous108376248
1170617450170617451AG56GENICheterozygous109166821
1170617460170617461GA53GENICheterozygous109346561
1170617466170617467GA54GENICheterozygous109346562
1170618661170618662GA20GENIChomozygous109166823
1170619031170619032CT26GENIChomozygous108376254
1170620820170620821TG40GENIChomozygous108376258
1170622757170622758TC19GENIChomozygous108376262
1170629034170629035CT15GENIChomozygous109166825