chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
9115933450115933451TC44GENIChomozygous117648964
9115933704115933705CT26GENIChomozygous117433329
9115933706115933707CT26GENIChomozygous117433330
9115933710115933711CT28GENICheterozygous117433331
9115933711115933712AG29GENICheterozygous117433332
9115941292115941293GA38GENICheterozygous117433333
9115960946115960947CA37GENICpossibly homozygous117648966
9116015992116015993AT46GENIChomozygous117648967
9116016001116016002GC46GENIChomozygous117648968
9116016010116016011TC49GENIChomozygous117648969
9116016021116016022GC44GENIChomozygous117648970
9116028023116028024AG18GENIChomozygous117433339
9116028025116028026AG19GENICpossibly homozygous117433340
9116028091116028092CA43GENIChomozygous117648971
9116028105116028106CG53GENIChomozygous117648972
9116028131116028132CA50GENIChomozygous117648973