chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2254963475254963476TC39GENIChomozygous59518828
2254963729254963730CT26GENIChomozygous59518830
2254963918254963919AG41GENIChomozygous59518832
2254964480254964481CG35GENIChomozygous59518834
2254964883254964884AG30GENIChomozygous59518836
2254965055254965056AC50GENIChomozygous59518838
2254965262254965263TC39GENIChomozygous59518840
2254965592254965593TG43GENIChomozygous59518842
2254965620254965621TC44GENIChomozygous59518844
2254965682254965683AG35GENIChomozygous59518846
2254966076254966077AAACACAC20GENIChomozygous61129412
2254966720254966721TC39GENIChomozygous59518848
2254966961254966962GA27GENIChomozygous59518850
2254967943254967944TA43GENIChomozygous59518851
2254968156254968157CT48GENIChomozygous59518853
2254968520254968521TC32GENIChomozygous59518855
2254969268254969269AG9GENIChomozygous59518857
2254969410254969411A-51GENIChomozygous59518859
2254970302254970303TC39GENIChomozygous59518861
2254971490254971491GA25GENICpossibly homozygous59518867
2254973710254973713AAA---10GENICpossibly homozygous59518876
2254973730254973731GGA11GENICpossibly homozygous59518880
2254973730254973731GGAA11GENICheterozygous60178196
2254974521254974522TC25GENIChomozygous59518882
2254974901254974902AG38GENIChomozygous59518890
2254975888254975889CG22GENIChomozygous59518892
2254976033254976034CCA26GENIChomozygous59518894
2254977780254977781CT27GENIChomozygous59518896
2254977952254977953TC22GENIChomozygous59518898
2254978356254978357CT29GENIChomozygous59518900
2254978758254978759CT2GENIChomozygous60688404
2254979208254979209A-32GENICpossibly homozygous59518902
2254979838254979839GA9GENIChomozygous59518904
2254974791254974792A-30GENICheterozygous60526508
2254972096254972097A-11GENICpossibly homozygous60526506
2254974790254974792AA--30GENICpossibly homozygous60526507