chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
196831407068314071CCA12GENIChomozygous46301299
196831438868314389AG21GENICpossibly homozygous46301300
196831460568314606GA21GENIChomozygous46196617
196831464468314645TC22GENICpossibly homozygous46196618
196831553968315540GT15GENICpossibly homozygous46196620
196831620968316210GA16GENIChomozygous46301301
196831765268317653GT10GENIChomozygous46301302
196831765968317660AT9GENIChomozygous46301303
196831839968318400CT21GENIChomozygous46196622
196831848368318484CT12GENIChomozygous46301304
196831857668318577AG14GENIChomozygous46196623
196831933768319338CT23GENICpossibly homozygous46196625
196831976768319768GGGACACCCTCCCTGCT2GENICheterozygous46196627
196832009168320092TC30GENICpossibly homozygous46301305
196832294868322949AT20GENICpossibly homozygous46301307
196832354568323546TC21GENIChomozygous46301308
196832376468323765TC21GENICpossibly homozygous46301309
196832441968324420TA25GENIChomozygous46301310
196832671368326714TC7GENIChomozygous46301314
196832681068326811AC8GENICpossibly homozygous46301315
196832765068327651CG17GENICpossibly homozygous46301316