chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7116928822116928823AC15GENIChomozygous967178282
7116930571116930572TC33GENIChomozygous967178283
7116930950116930951TC34GENIChomozygous967178284
7116931640116931641TC19GENIChomozygous967178285
7116933057116933058AT39GENIChomozygous967178286
7116933972116933973AG30GENIChomozygous967178287
7116934411116934412GA35GENIChomozygous967178288
7116935780116935781GT24GENIChomozygous967178289
7116937285116937286GT41GENIChomozygous967178290
7116939739116939740TG42GENICpossibly homozygous967178291
7116941317116941318TC52GENIChomozygous967178292
7116941720116941721CA17GENIChomozygous967178293
7116941721116941722TG17GENIChomozygous967178294