chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
9119307269119307270AG33GENIChomozygous117653184
9119307940119307941TC24GENIChomozygous117653185
9119309769119309770TC60GENIChomozygous117653186
9119310000119310001AG39GENIChomozygous117653187
9119310338119310339TA38GENIChomozygous117653188
9119310574119310575TC42GENIChomozygous117653189
9119310860119310861CT55GENIChomozygous117653190
9119311324119311325AG49GENIChomozygous117653191
9119308522119308522GAG33GENIChomozygous128752485
9119311175119311175ATAA43GENIChomozygous128752486
9119311424119311425T35GENIChomozygous128752487
9119312604119312605CT28GENIChomozygous117653192
9119312906119312907GA34GENIChomozygous117445232
9119313210119313211TC49GENIChomozygous117653193
9119313366119313367TC56GENIChomozygous117653194
9119313651119313652GA52GENIChomozygous117653195
9119313770119313771TC49GENIChomozygous117653196
9119313843119313844AG55GENIChomozygous117653197
9119314259119314260CT56GENIChomozygous117653198
9119314270119314271CT52GENIChomozygous117653199
9119314447119314447AC26GENICpossibly homozygous128752488
9119314530119314530CG52GENIChomozygous128752489
9119314668119314669TG36GENIChomozygous117653200
9119314820119314821CT50GENIChomozygous117653201
9119315230119315231CT48GENIChomozygous117653202
9119316171119316172TC55GENICpossibly homozygous117653203
9119316522119316522T43GENIChomozygous128752490
9119316605119316605CA46GENIChomozygous128752491
9119317915119317928GTGGCGGGGGGGC14GENIChomozygous128752492
9119317936119317938GT15GENIChomozygous128752493
9119318310119318311T29GENIChomozygous128752494
9119318475119318476AT40GENIChomozygous117653204
9119318711119318722TTTTTTTTTTG27GENICheterozygous128752495
9119319358119319359AG42GENIChomozygous117653205
9119320234119320234CC29GENIChomozygous128752496
9119320815119320816TC42GENIChomozygous117653208
9119320114119320115AC53GENICpossibly homozygous117653206
9119320462119320463CA37GENICpossibly homozygous117653207