chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1198323509198323510CT27GENIChomozygous108497469
1198324291198324292CT20GENIChomozygous108497471
1198324675198324676AG27GENIChomozygous108497473
1198324729198324730TC28GENIChomozygous108497475
1198325610198325611AT30GENIChomozygous108497477
1198325763198325764GA32GENIChomozygous108497479
1198325944198325945AT34GENIChomozygous108497481
1198329922198329923CT22GENIChomozygous108497483
1198331125198331126TC27GENIChomozygous108497485
1198331991198331992TC20GENIChomozygous108497487
1198333861198333862GT27GENIChomozygous108497489
1198329327198329328A18GENIChomozygous127472225
1198330874198330890TCTCTCTCTCTCTCTT25GENICheterozygous127472226
1198336166198336167T24GENIChomozygous127472227
1198340182198340183GA15GENICpossibly homozygous108497491
1198342343198342344GA20GENIChomozygous108497493
1198343325198343326TC24GENIChomozygous108497495
1198343686198343686GAGGGAGGAGGAGGGGA9GENIChomozygous127472228
1198345807198345808AG26GENIChomozygous108497499
1198346393198346394TG21GENIChomozygous108497501
1198346619198346620GA20GENIChomozygous108497503
1198346972198346973GA33GENIChomozygous108497505
1198348040198348041AC24GENIChomozygous108497507
1198348210198348211CA16GENIChomozygous108497509
1198348211198348212AT17GENIChomozygous108497511
1198348859198348860GA25GENIChomozygous108497513
1198348988198348989T19GENICheterozygous131581218
1198349321198349322GA34GENIChomozygous108497515
1198353617198353618TC28GENIChomozygous108497517
1198354225198354226CG23GENIChomozygous108497519
1198354409198354410GT21GENICpossibly homozygous108497521
1198355028198355028T26GENIChomozygous127472230