chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135045592450455925TC26GENIChomozygous980164002
135045626150456262CT50GENIChomozygous980164003
135045683450456835CT64GENIChomozygous980164004
135045712850457129AT14GENIChomozygous980164005
135045761750457618GT39GENICpossibly homozygous980164006
135045811150458112GC40GENIChomozygous980164007
135045816050458161GA37GENIChomozygous980164008
135045890550458906CT33GENIChomozygous980164009
135045928450459285CG74GENIChomozygous980164010
135046119150461192TA62GENIChomozygous980164011
135046151050461511AT72GENIChomozygous980164012
135046158650461587TA74GENIChomozygous980164013
135046200850462009CT42GENIChomozygous980164014
135046234050462341CT35GENIChomozygous980164015
135046240150462402GA43GENIChomozygous980164016
135046240350462404CT44GENIChomozygous980164017
135046240550462406GT44GENIChomozygous980164018
135046360050463601CT33GENIChomozygous980164019
135046388650463887CT23GENIChomozygous980164020
135046431650464317CT38GENIChomozygous980164021
135046548850465489TC36GENIChomozygous980164022
135046559150465592AC36GENIChomozygous980164023
135046566250465663AG46GENIChomozygous980164024
135046587050465871TC72GENIChomozygous980164025
135046594750465948GA61GENIChomozygous980164026
135046639850466399AT5GENIChomozygous980164027
135046645450466455GA21GENIChomozygous980164028
135046656550466566GA37GENIChomozygous980164029
135046817550468176AG70GENIChomozygous980164030
135046926350469264AG52GENIChomozygous980164031
135047180550471806AG60GENIChomozygous980164032
135047184150471842AG80GENIChomozygous980164033
135047197950471980TC87GENIChomozygous980164034
135047459350474594CT38GENIChomozygous980164035
135047628250476283TC60GENIChomozygous980164036
135047645850476459CT39GENIChomozygous980164037
135047836750478368GA52GENIChomozygous980164038
135047848750478488CT42GENIChomozygous980164039
135047869550478696CT47GENIChomozygous980164040
135047898150478982CT26GENIChomozygous980164041