chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
195627592356275924GA10GENICpossibly homozygous119633749
195627653456276535CG26GENIChomozygous109738316
195627748256277483GA23GENIChomozygous109738318
195627907056279071CT21GENIChomozygous109738320
195628142456281425AG37GENIChomozygous109738322
195628148756281488TC30GENIChomozygous109738324
195628297956282980GA30GENIChomozygous109738326
195628407156284072TG35GENIChomozygous109738328
195628442756284428CT14GENIChomozygous109738330
195628816456288165CG35GENIChomozygous109738332
195628820056288201GA34GENIChomozygous109738334
195628825656288257GA32GENICpossibly homozygous109738336
195629141156291412CG26GENIChomozygous109738338
195629174756291748GT33GENIChomozygous109738340
195629233256292333AG28GENIChomozygous109738342
195629373056293731CT30GENIChomozygous109738344
195629399856293999GA35GENIChomozygous109738346
195629412356294124CT20GENIChomozygous109738348
195629479256294793TC34GENIChomozygous109738350
195629483356294834GA24GENIChomozygous109738352
195629500056295001CT30GENIChomozygous109738354
195629533056295331AG13GENIChomozygous109738356
195629533356295334TC14GENIChomozygous109738358
195629668856296689CT22GENIChomozygous109738360
195628851456288515TC36GENIChomozygous109789132