chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
146113699461136995AG9GENICpossibly homozygous113787884
146113769461137695GC28GENIChomozygous113476870
146113881761138818TC33GENICpossibly homozygous114123229
146113931961139320AG30GENIChomozygous113476872
146113985561139856CT25GENIChomozygous113476874
146113936361139364TC30GENIChomozygous113743493
146114330261143303CT20GENICpossibly homozygous114123233
146116419561164196TA36GENICpossibly homozygous114123235
146116423461164235GA30GENIChomozygous114123237
146117005961170060AG20GENIChomozygous114123243
146116441361164414TC23GENICpossibly homozygous113476880
146116943261169433GT21GENIChomozygous114123241
146114347861143479AC5GENICheterozygous114181749
146117147561171476CA21GENIChomozygous114123245
146117283961172840AG20GENIChomozygous114123247
146117361461173615GA28GENIChomozygous113476884
146117425261174253CG18GENIChomozygous113476886