chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1170600356170600357CA20GENIChomozygous109166817
1170600843170600844GA7GENIChomozygous109166819
1170601709170601710AT17GENIChomozygous108376219
1170606236170606237AG29GENIChomozygous108376223
1170606331170606332TG8GENICheterozygous120509324
1170606333170606334CG8GENICheterozygous120509325
1170610794170610795AG20GENIChomozygous108376238
1170618661170618662GA29GENIChomozygous109166823
1170619031170619032CT24GENIChomozygous108376254
1170620820170620821TG30GENIChomozygous108376258
1170622191170622192GT11GENICheterozygous120509326
1170622757170622758TC17GENIChomozygous108376262