chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1214284118214284119TC14GENIChomozygous801735284
1214286276214286277TA10GENIChomozygous801735285
1214286351214286352AG23GENICheterozygous801735286
1214287703214287704AG45GENICheterozygous801735287
1214287709214287710AG48GENICheterozygous801735288
1214287736214287737GA50GENICheterozygous801735289
1214287745214287746AG51GENICheterozygous801735290
1214288411214288412GA35GENICheterozygous801735291
1214288462214288463GA47GENICheterozygous801735292
1214291148214291149AG19GENIChomozygous801735293
1214291223214291224GA20GENICheterozygous801735294
1214293084214293085AG22GENIChomozygous801735295
1214296633214296634TC34GENIChomozygous801735296
1214299976214299977CT12GENIChomozygous801735297
1214301593214301594TC18GENIChomozygous801735298
1214302573214302574CT32GENIChomozygous801735299
1214311167214311168AG30GENIChomozygous801735300
1214313215214313216TA32GENICpossibly homozygous801735301
1214313464214313465TC21GENIChomozygous801735302