chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
187295266572952666TA37GENICheterozygous119501310
187295358972953590GT59GENICpossibly homozygous110499326
187295404072954041AC20GENIChomozygous110400479
187295440772954408GA53GENIChomozygous110400481
187295518272955183GC37GENICheterozygous119501311
187295526072955261AG54GENIChomozygous110400483
187295531972955320AG45GENIChomozygous110400485
187295643172956432GA54GENIChomozygous110400487
187295734172957342CA55GENIChomozygous110400489
187295740072957401CA62GENIChomozygous110400491
187295757472957575AG34GENIChomozygous110400493
187295773072957731CT28GENIChomozygous110400495
187295824672958247TC49GENIChomozygous110400497
187295857572958576CA12GENIChomozygous119501312
187295860572958606CT5GENICheterozygous119501313
187295886072958861GA39GENICpossibly homozygous110499330
187295889272958893TA50GENICpossibly homozygous110499332
187295910472959105CA46GENIChomozygous110400499
187295940472959405GA51GENIChomozygous110400501
187296076872960769AT36GENICpossibly homozygous110693178
187296116872961169CT32GENICheterozygous119501314
187296167872961679AG62GENIChomozygous110400503
187296235672962357AT41GENIChomozygous110400505
187296257372962574CT63GENIChomozygous110400507
187296262272962623CT63GENIChomozygous110400509