chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5144441162144441163A-20GENIChomozygous56068152
5144441662144441663TC26GENIChomozygous55762318
5144441858144441859TC21GENIChomozygous55762322
5144441865144441866TC20GENIChomozygous55762324
5144442554144442555CT10GENIChomozygous56068153
5144443151144443152CT12GENIChomozygous56068154
5144443215144443216TC21GENIChomozygous55762326
5144443453144443454CT12GENIChomozygous55762327
5144443940144443955CCCCCCCCCCCCCCC---------------11GENIChomozygous56589317
5144443954144443955CCTTTTTTTTTTT10GENIChomozygous56589318
5144443967144443968G-13GENIChomozygous55762335
5144444054144444055GA22GENIChomozygous55762337
5144444284144444297CAAAAAAAAAAAA-------------6GENICheterozygous55762340
5144444316144444317G-8GENIChomozygous55762342
5144444320144444321TC12GENIChomozygous55762344
5144444328144444329TTGAGGAGGAG16GENIChomozygous55762346
5144444743144444744AG12GENIChomozygous55762348
5144444829144444830AG13GENIChomozygous55762352
5144444887144444888AG3GENIChomozygous55762357
5144445317144445319TT--28GENICpossibly homozygous55762361
5144445383144445384CT29GENIChomozygous56068156
5144445911144445912TC29GENIChomozygous56068157
5144445912144445913GA29GENIChomozygous56068158
5144445943144445944CT26GENIChomozygous56068159
5144446248144446249AG18GENIChomozygous55762367
5144446497144446498AC19GENIChomozygous56068160
5144446983144446984GA15GENIChomozygous56068161
5144447004144447005CA17GENIChomozygous56068162
5144444859144444860CCTTTTTTT9GENIChomozygous56458649