chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103791787537917876AG20GENIChomozygous138768583
103791800937918010TC18GENIChomozygous138768584
103791803037918031T18GENIChomozygous146934314
103791824537918246CA23GENIChomozygous138768585
103791849637918497TC21GENIChomozygous146951999
103791913737919138GC32GENICpossibly homozygous146952000
103791960437919605TC26GENIChomozygous138768586
103792013637920137CT28GENIChomozygous146952001
103792037337920374GA23GENIChomozygous138768587
103792221137922212TC21GENIChomozygous146952002
103792230637922306TTG17GENIChomozygous146934315
103792271337922714AG23GENIChomozygous138768591
103792276237922763GA24GENIChomozygous146952003
103792398737923988TG21GENIChomozygous138768592
103792408937924090CT21GENIChomozygous146952004