chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85083222950832230TG48GENICpossibly homozygous53206179
85083239350832395GT--22GENIChomozygous53206180
85083244550832449CTTC----22GENIChomozygous53206181
85083245850832459CA28GENIChomozygous53116309
85083253350832534TC24GENIChomozygous53116310
85083259850832599TG22GENIChomozygous53206182
85083297450832976AC--18GENIChomozygous53116313
85083298750832988CT23GENICpossibly homozygous53206183
85083302950833031AC--22GENIChomozygous53116315
85083303050833031CT27GENICpossibly homozygous53206184
85083306550833067TG--20GENIChomozygous53206185
85083310550833106TG26GENICpossibly homozygous53206186
85083310750833108TG26GENICpossibly homozygous52626064
85083327650833277TTA31GENIChomozygous53206187
85083332850833329CT33GENIChomozygous53206188
85083342850833429TA37GENIChomozygous53116318
85083344350833444TC37GENIChomozygous53116319
85083418750834188GA33GENIChomozygous53206189
85083421650834217C-35GENIChomozygous53206190
85083461650834617CT25GENIChomozygous53206191
85083493250834933GA27GENIChomozygous53116320
85083565650835657AG48GENIChomozygous53116322
85083628150836282CT36GENIChomozygous53116323
85083670550836706AC38GENIChomozygous53116324
85083683450836836AC--1GENIChomozygous52972477
85083728350837284GC32GENIChomozygous53116326
85083728650837287T-31GENIChomozygous53116327
85083762150837622TC44GENIChomozygous53116329
85083777250837773AG47GENIChomozygous53116330
85083794250837943GA29GENICpossibly homozygous53206192
85083838650838387TC35GENICpossibly homozygous53116332
85083845850838460AA--19GENICheterozygous53116334
85083862450838625AG33GENIChomozygous53206193
85083906550839066GA28GENICpossibly homozygous53206194
85083938350839384GA42GENIChomozygous53116337
85083944450839445TC43GENIChomozygous53116338