chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1103186861103186862CT25INTERGENIChomozygous75434513
1103187217103187218GA19INTERGENIChomozygous75434514
1103187218103187219CT18INTERGENIChomozygous75434515
1103187287103187288GT19INTERGENIChomozygous74265157
1103187971103187972AT13INTERGENIChomozygous74265166
1103188147103188148GA14INTERGENIChomozygous74265168
1103188293103188294GA16INTERGENIChomozygous74265171
1103188494103188495TC13INTERGENIChomozygous74265174
1103188508103188509CA13INTERGENIChomozygous74265177
1103188542103188543TC18INTERGENIChomozygous74265180
1103188550103188551AG17INTERGENIChomozygous74265183
1103188636103188637AG11INTERGENIChomozygous74265186
1103188706103188707TC5INTERGENIChomozygous74265189
1103188710103188711GA5INTERGENIChomozygous74265192
1103188908103188909TC14INTERGENIChomozygous74265195
1103188944103188945TG22INTERGENICheterozygous74265198
1103189135103189136TG9INTERGENICheterozygous74265207
1103189251103189252AG15INTERGENIChomozygous74265210
1103189326103189327TC17INTERGENIChomozygous74265213
1103189367103189368CA15INTERGENIChomozygous75103345
1103189233103189234AG9INTERGENIChomozygous75103343
1103189368103189369GA15INTERGENIChomozygous75103347
1103189376103189377TG16INTERGENICheterozygous75103349
1103189487103189488TG27INTERGENIChomozygous75103351
1103189496103189497AC27INTERGENIChomozygous74265216
1103189527103189528AG16INTERGENIChomozygous75103353
1103189574103189575TG11INTERGENICheterozygous75103355
1103189792103189793CT23INTERGENIChomozygous75103359
1103189854103189855TC24INTERGENIChomozygous75103361
1103189935103189936AT29INTERGENIChomozygous75434517
1103189966103189967TG38INTERGENIChomozygous75103363
1103190287103190288TG22INTERGENIChomozygous75103367
1103190375103190376TC28INTERGENIChomozygous75103371
1103190443103190444CT25INTERGENIChomozygous75103373