chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4145195721145195722AG19GENIChomozygous112870704
4145197271145197272AG35GENIChomozygous119315322
4145197305145197306TC29GENIChomozygous119315323
4145197918145197919AG28GENIChomozygous112870705
4145198516145198517TC13GENIChomozygous119315324
4145201765145201766TC17GENIChomozygous112870707
4145203093145203094CT34GENIChomozygous119315325
4145204160145204161CT27GENIChomozygous119315326
4145204570145204571AG8GENIChomozygous119412347
4145205104145205105AC14GENIChomozygous119315327
4145206300145206301AG29GENIChomozygous119315328
4145207559145207560CT20GENIChomozygous119315329
4145208138145208139TC19GENIChomozygous112870709
4145222351145222352TG18GENIChomozygous119315330
4145213384145213385TC18GENIChomozygous112870711
4145215748145215749TC33GENIChomozygous112870712
4145218784145218785AG26GENIChomozygous112870713
4145222743145222744TC13GENIChomozygous119315331
4145222926145222927TC19GENIChomozygous119315332
4145224901145224902CG19GENIChomozygous119315333
4145225194145225195TC21GENIChomozygous112870716
4145225273145225274CT27GENICpossibly homozygous119315334
4145225920145225921AG27GENIChomozygous112870717
4145232701145232702GC15GENIChomozygous112870718
4145233671145233672CT25GENIChomozygous119315335
4145233918145233919TC32GENIChomozygous119315336
4145234556145234557CT28GENIChomozygous119315337
4145235080145235081TG27GENIChomozygous119315338
4145236330145236331TC38GENIChomozygous119315339
4145236399145236400AG28GENIChomozygous112870723