chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71434151414341515CG34GENICheterozygous115575394
71434174214341743CA31GENICpossibly homozygous116317442
71434242314342424CT26GENIChomozygous115575395
71434619714346198GT10GENIChomozygous115575396
71434803614348037GA34GENIChomozygous115575397
71434843214348433GA25GENIChomozygous115575398
71434932914349330AT24GENICheterozygous115575399
71435098114350982GA30GENIChomozygous115575400
71435618514356186CT42GENIChomozygous115575401
71436002014360021GC38GENIChomozygous115575402
71436149914361500CG12GENIChomozygous115575403
71436178914361790CT33GENIChomozygous115575404
71436256514362566AT27GENIChomozygous115575405
71436296214362963CA34GENICheterozygous115575406
71436297014362971AC35GENICpossibly homozygous115575407
71436327814363279AG16GENIChomozygous115575408
71436902014369021AG20GENIChomozygous115575409
71436967414369675TC33GENIChomozygous115575410
71436107414361075CA6GENIChomozygous116004307