chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122141387321413874TA39GENICheterozygous804306214
122141388421413885AG26GENICheterozygous804306215
122141392321413924GA29GENIChomozygous804306216
122141396121413962CA34GENICheterozygous804306217
122141403021414031TC52GENIChomozygous804306218
122141405421414055AT57GENIChomozygous804306219
122141409321414094GA46GENIChomozygous804306220
122141420621414207CT24GENIChomozygous804306221
122141424421414245AT18GENIChomozygous804306222
122141438521414386CT53GENIChomozygous804306223
122141439021414391GA51GENIChomozygous804306224
122141441421414415GA54GENIChomozygous804306225
122141454321414544AG72GENIChomozygous804306226
122141457321414574AC65GENIChomozygous804306227
122141469621414697TA48GENIChomozygous804306228
122141472721414728CA49GENICheterozygous804306229
122141475921414760AG60GENICheterozygous804306230
122141479021414791GA71GENICheterozygous804306231
122141486221414863GA62GENICheterozygous804306232
122141512621415127GA23GENICheterozygous804306233
122141512921415130AG22GENIChomozygous804306234
122141604421416045TC64GENIChomozygous804306235
122141606321416064AG69GENIChomozygous804306236
122141614821416149CT36GENIChomozygous804306237
122141628621416287AC2GENIChomozygous804306238
122141648121416482TC18GENIChomozygous804306239
122141650621416507GA33GENIChomozygous804306240
122141662921416630GA62GENIChomozygous804306241
122141665821416659AG58GENIChomozygous804306242
122141671821416719CT26GENICheterozygous804306243
122141680921416810CT18GENIChomozygous804306244
122141708521417086AT36GENIChomozygous804306245
122141717321417174GA39GENIChomozygous804306246
122141720221417203AC49GENIChomozygous804306247
122141735921417360TG66GENIChomozygous804306248