chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
726059402605941CT58GENIChomozygous118344013
726074532607453CTCT53GENIChomozygous133169197
726091912609192AG63GENIChomozygous118399294
726074602607461TC53GENIChomozygous115545462
726081632608164CT61GENIChomozygous115545464
726085702608571AC57GENIChomozygous115545466
726089262608926A45GENIChomozygous128432304
726102082610209CA51GENIChomozygous118344014
726103102610311GA49GENIChomozygous118344015
726104472610447TTTA43GENIChomozygous133169198
726105392610540CG32GENIChomozygous118344016
726105902610591TC37GENIChomozygous118344017
726109192610919T36GENIChomozygous128432306
726114362611437CT36GENIChomozygous118344018
726114562611457CG45GENIChomozygous115545468
726117612611762TG41GENIChomozygous118344019
726122472612248AG69GENIChomozygous115545470
726127052612705A59GENIChomozygous131006974
726128682612868T10GENIChomozygous133169199
726128782612878GTGGCAGCC5GENIChomozygous133169200
726100002610001TG25GENIChomozygous133176148
726148832614884GA11GENIChomozygous116311299
726150732615074GA38GENIChomozygous118344020
726152822615282A33GENIChomozygous131006978
726159682615969AG46GENIChomozygous115545472
726178202617821AC42GENIChomozygous118344021
726187922618793TC61GENIChomozygous115545474
726188572618857T55GENICpossibly homozygous133169201
726188732618874TG65GENIChomozygous133176149
726204922620493TC50GENIChomozygous118344022
726206462620646G32GENIChomozygous133169202
726207302620731CA49GENIChomozygous118344023
726216362621637CT53GENIChomozygous118344024