chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1103186861103186862CT33INTERGENIChomozygous75434513
1103187217103187218GA21INTERGENIChomozygous75434514
1103187218103187219CT20INTERGENIChomozygous75434515
1103187287103187288GT27INTERGENIChomozygous74265157
1103187803103187804AC17INTERGENIChomozygous75103339
1103187971103187972AT24INTERGENIChomozygous74265166
1103188147103188148GA37INTERGENIChomozygous74265168
1103188293103188294GA36INTERGENIChomozygous74265171
1103188494103188495TC28INTERGENIChomozygous74265174
1103188508103188509CA24INTERGENIChomozygous74265177
1103188542103188543TC25INTERGENIChomozygous74265180
1103188550103188551AG25INTERGENIChomozygous74265183
1103188636103188637AG27INTERGENIChomozygous74265186
1103188706103188707TC20INTERGENIChomozygous74265189
1103188710103188711GA21INTERGENIChomozygous74265192
1103188908103188909TC24INTERGENIChomozygous74265195
1103188944103188945TG26INTERGENICheterozygous74265198
1103189135103189136TG16INTERGENICheterozygous74265207
1103189233103189234AG11INTERGENIChomozygous75103343
1103189251103189252AG17INTERGENIChomozygous74265210
1103189326103189327TC13INTERGENIChomozygous74265213
1103189367103189368CA4INTERGENIChomozygous75103345
1103189368103189369GA3INTERGENIChomozygous75103347
1103189376103189377TG4INTERGENIChomozygous75103349
1103189487103189488TG21INTERGENICpossibly homozygous75103351
1103189496103189497AC18INTERGENIChomozygous74265216
1103189527103189528AG17INTERGENIChomozygous75103353
1103189574103189575TG18INTERGENIChomozygous75103355
1103189792103189793CT22INTERGENIChomozygous75103359
1103189854103189855TC30INTERGENIChomozygous75103361
1103189935103189936AT21INTERGENIChomozygous75434517
1103189966103189967TG21INTERGENIChomozygous75103363
1103190287103190288TG16INTERGENIChomozygous75103367
1103190375103190376TC10INTERGENIChomozygous75103371
1103190443103190444CT18INTERGENIChomozygous75103373