chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
173068241430682415CT55GENICpossibly homozygous111344857
173068426430684265CT55GENIChomozygous111344859
173068597230685973AT47GENIChomozygous133314385
173068748430687485TC54GENIChomozygous111023389
173068971330689714G62GENIChomozygous129442255
173069103630691037T33GENIChomozygous129442256
173069132730691328CT55GENICpossibly homozygous111344863
173069174630691747CG40GENIChomozygous111023395
173069254030692541CA45GENIChomozygous111344865
173069288430692885TG54GENIChomozygous111023397
173069428730694288G35GENIChomozygous129442258
173069444130694441T34GENIChomozygous129442259
173069444530694445T33GENIChomozygous129442260
173069447230694472T25GENIChomozygous129442262
173069448030694481G22GENIChomozygous129442263
173069459930694600TC40GENIChomozygous111023399
173069490830694909AG51GENIChomozygous111023401
173069827130698272AG63GENIChomozygous111344867
173069985630699857TC31GENIChomozygous111344869
173069676930696770AG45GENIChomozygous111499390
173070336930703370GA45GENICpossibly homozygous111023419
173070549430705495CT32GENIChomozygous119423344
173070686230706863TC52GENIChomozygous111023421
173070853330708534AG42GENIChomozygous133314386
173070917830709179CT31GENIChomozygous111344871
173070948230709483AG41GENIChomozygous111344873
173070962630709627CT57GENIChomozygous111023425
173070992330709924AG39GENIChomozygous111023427
173071222630712227CT39GENIChomozygous111023431
173071230930712310A58GENICpossibly homozygous129442267
173070546230705462TAGATAGATAGATAGATAGATAGA19GENIChomozygous133310724
173071257830712578T51GENIChomozygous133310725
173071003230710032T17GENICheterozygous131529295