chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
11285798812857989CT30GENIChomozygous147897400
11286081812860819CT34GENIChomozygous147897401
11286140312861404CT27GENIChomozygous147897402
11286211012862111AG22GENIChomozygous135505437
11286224612862247TC32GENIChomozygous135505438
11286231612862317TC24GENIChomozygous135505439
11286291912862920GA24GENIChomozygous147897403
11286294512862946GA29GENIChomozygous147897404
11286311312863114CT28GENIChomozygous147897405
11286367612863677CT13GENIChomozygous135505443
11286371412863715TC13GENIChomozygous147897406
11286366512863667GC13GENIChomozygous135395482
11286411612864117GC34GENIChomozygous135505445
11286651812866519GA34GENIChomozygous147897407
11286722812867229AG25GENICpossibly homozygous135505447
11286723112867232AG25GENICpossibly homozygous135505448
11286788312867884TC24GENIChomozygous135505449
11286801812868019AC21GENIChomozygous135505450
11286822612868227CT22GENIChomozygous147897408
11286873212868732AAAT20GENIChomozygous135395489
11286876512868767GT28GENIChomozygous135395490
11286983012869831TA30GENIChomozygous147897409
11287030512870306AG29GENIChomozygous135505452
11286376712863767GC14GENIChomozygous147887739
11286378512863785GC17GENIChomozygous147887740
11286380712863807GT21GENIChomozygous147887741
11286384612863847CT23GENIChomozygous147769905