chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1797780229778023TC14GENIChomozygous111524240
1797783949778395TG10GENIChomozygous110953097
1797792519779252TA13GENIChomozygous111524241
1797800849780085GT23GENIChomozygous111230206
1797808899780890AG26GENIChomozygous110953099
1797810219781022CG21GENIChomozygous110953101
1797826459782646TA7GENIChomozygous111524242
1797826579782658CA7GENIChomozygous111524243
1797828489782849AG17GENIChomozygous110953117
1797831439783144AG14GENIChomozygous111524244
1797834669783467TC10GENIChomozygous111524245
1797837649783765AT7GENIChomozygous111524246
1797837679783768CA6GENIChomozygous111524247
1797839109783911TA7GENIChomozygous111524248
1797841169784117GT10GENIChomozygous111524249
1797841539784154GT5GENIChomozygous111230212
1797847629784763AG4GENIChomozygous111524250
1797849299784930TC3GENIChomozygous111524251
1797850959785096AG6GENIChomozygous111524252
1797852219785222CT3GENIChomozygous111524253
1797855759785576AG10GENIChomozygous111524255
1797862089786209CT19GENIChomozygous111524257
1797862489786249AG19GENIChomozygous111524259
1797866129786613TC22GENIChomozygous110953119
1797875459787546TA31GENIChomozygous110953125
1797885399788540GC4GENIChomozygous111524261
1797888329788833AT24GENIChomozygous111332216
1797803379780338AC19GENIChomozygous111166990
1797893469789347GC19GENICpossibly homozygous110953127
1797894569789457CT18GENIChomozygous110953129
1797895069789507CA17GENIChomozygous110953131
1797895219789522TC13GENIChomozygous110953133
1797898809789881GA19GENIChomozygous110953135
1797900439790044GA15GENIChomozygous110953137
1797902849790285GA18GENIChomozygous110953141
1797903889790389AG23GENIChomozygous111524263
1797907909790791GA17GENIChomozygous110953143
1797913919791392CT10GENIChomozygous110953145
1797918709791871CT11GENIChomozygous111524265
1797919289791929GA8GENIChomozygous110953147