chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3109753866109753867AG28GENIChomozygous141529260
3109753974109753975CT20GENIChomozygous141529261
3109755424109755425TC21GENIChomozygous136788319
3109755532109755533AG17GENIChomozygous141529262
3109756329109756330GA23GENIChomozygous141529263
3109756526109756527TA14GENIChomozygous141529264
3109757503109757504CG23GENIChomozygous141529265
3109757749109757750GA21GENIChomozygous141529266
3109758923109758924TC17GENIChomozygous141529267
3109760782109760783AG12GENIChomozygous136788320
3109766280109766281CT15GENIChomozygous136788323
3109766994109766995GT20GENIChomozygous141529268
3109767303109767304CT14GENIChomozygous136788324
3109762405109762407GT31GENIChomozygous136583629
3109760492109760496TACT14GENIChomozygous141479395
3109762220109762221A10GENIChomozygous141479396
3109765428109765429AG2GENICheterozygous149489653
3109765430109765431AG2GENICheterozygous149489654
3109765433109765434AT3GENICheterozygous149489655
3109769178109769179AG24GENIChomozygous136788326
3109769476109769483AAAAGAA10GENIChomozygous136583631
3109769946109769947GA2GENIChomozygous141529269
3109770218109770219CT24GENIChomozygous141529270
3109770854109770855AG27GENIChomozygous136788328
3109772251109772252AG22GENIChomozygous141529271
3109773177109773178TC33GENIChomozygous141529272
3109773449109773450TC22GENIChomozygous136788332
3109774381109774382CT24GENIChomozygous141529273