chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
184595804045958041TG16GENIChomozygous119491447
184598535045985351TC11GENICpossibly homozygous110331255
184599916545999166CT6GENIChomozygous110331257
184600001746000018CT23GENIChomozygous110331259
184603586246035863GC12GENIChomozygous110331261
184605927746059278TC10GENIChomozygous110331263
184606295546062956GT13GENICheterozygous119553826
184606439346064394GA31GENIChomozygous110331265
184612553346125534CT14GENIChomozygous110331267
184613381846133819GA18GENIChomozygous110331269
184614961746149618CT23GENIChomozygous110331271