chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
26094999760949998CT61GENIChomozygous109781178
26095070060950701AG58GENIChomozygous109781180
26095103260951033AG58GENIChomozygous109781181
26095156360951564TC60GENIChomozygous109781183
26095190660951907GA60GENIChomozygous109781185
26095312260953123AG45GENICpossibly homozygous109781188
26095426760954268CG58GENIChomozygous109781190
26095451960954520CT47GENIChomozygous109781192
26095508860955089GA52GENIChomozygous109781194
26095509160955092GA52GENIChomozygous109781196
26095564360955644GC53GENICpossibly homozygous109781198
26095576160955762AG48GENIChomozygous109781200
26095602460956025AG39GENIChomozygous109781202
26095610360956104GA41GENIChomozygous109781204
26095623760956238AG56GENIChomozygous109781205
26095639160956392CT33GENIChomozygous109781207
26095641460956415GA26GENIChomozygous109781209
26095655660956557AC28GENIChomozygous109781211
26095663860956639AG37GENIChomozygous109781213
26095680860956809TG55GENIChomozygous109781215
26095697660956977TA52GENIChomozygous109781217
26095699160956992GA60GENIChomozygous109781219
26095702160957022GA59GENICpossibly homozygous109781221
26095750160957502TC53GENIChomozygous109781223
26095754160957542CT60GENIChomozygous109781225
26095813360958134TC55GENIChomozygous109781227
26095853860958539GT51GENIChomozygous109781229
26095891060958911TC53GENIChomozygous109781231
26095893660958937GA57GENIChomozygous109781233
26095933160959332AG42GENIChomozygous109781235
26095947360959474CT50GENIChomozygous109781237
26095955060959551CT57GENIChomozygous109781239
26095960060959601CA56GENIChomozygous109781240
26096016360960164AC32GENIChomozygous109781241
26096044360960444TC64GENIChomozygous109781243
26096063760960638GA57GENIChomozygous109781245
26096079260960793CT49GENIChomozygous109781247
26096080860960809AT56GENICpossibly homozygous109781249
26096123360961234CT47GENIChomozygous109781251