chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3109753866109753867AG27GENIChomozygous141529260
3109753974109753975CT22GENIChomozygous141529261
3109755424109755425TC25GENIChomozygous136788319
3109755532109755533AG34GENIChomozygous141529262
3109756329109756330GA19GENIChomozygous141529263
3109756526109756527TA17GENIChomozygous141529264
3109757503109757504CG17GENIChomozygous141529265
3109757749109757750GA16GENIChomozygous141529266
3109758923109758924TC32GENIChomozygous141529267
3109760782109760783AG22GENIChomozygous136788320
3109766280109766281CT12GENIChomozygous136788323
3109766994109766995GT27GENIChomozygous141529268
3109767303109767304CT19GENIChomozygous136788324
3109769178109769179AG21GENIChomozygous136788326
3109762220109762221A18GENIChomozygous141479396
3109769476109769483AAAAGAA9GENIChomozygous136583631
3109762405109762407GT30GENIChomozygous136583629
3109760492109760496TACT23GENIChomozygous141479395
3109769946109769947GA8GENIChomozygous141529269
3109770218109770219CT28GENIChomozygous141529270
3109770854109770855AG16GENIChomozygous136788328
3109772251109772252AG28GENIChomozygous141529271
3109773177109773178TC14GENIChomozygous141529272
3109773449109773450TC27GENIChomozygous136788332
3109774381109774382CT27GENIChomozygous141529273