chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1170597358170597359GA73GENIChomozygous108376209
1170597788170597789GA61GENIChomozygous108376211
1170598294170598295TC33GENIChomozygous108376213
1170600154170600155CT26GENIChomozygous108376215
1170600834170600835CA79GENIChomozygous108376217
1170601709170601710AT15GENIChomozygous108376219
1170606236170606237AG91GENIChomozygous108376223
1170606965170606966CT40GENIChomozygous108376227
1170607688170607689CT90GENIChomozygous108376229
1170609062170609063CT41GENIChomozygous108376231
1170609109170609110TC63GENIChomozygous108376234
1170609945170609946TC34GENIChomozygous108376236
1170610794170610795AG13GENIChomozygous108376238
1170610870170610871CA17GENIChomozygous108376240
1170611061170611062CT35GENIChomozygous108376242
1170611828170611829CT44GENIChomozygous108376244
1170614080170614081AG76GENIChomozygous108376246
1170615839170615840CT40GENIChomozygous108376248
1170616208170616209CT42GENIChomozygous108376250
1170616360170616361CT30GENIChomozygous108376252
1170619031170619032CT28GENIChomozygous108376254
1170619252170619253CT13GENIChomozygous108376256
1170620820170620821TG32GENIChomozygous108376258
1170621609170621610GA43GENIChomozygous108376260
1170622757170622758TC21GENIChomozygous108376262
1170625577170625578CT30GENIChomozygous108376264
1170626457170626458GA20GENIChomozygous108376266
1170628428170628429TA56GENIChomozygous108958866