chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10110046708110046709AT19GENIChomozygous116719453
10110046912110046913AT8GENIChomozygous117201120
10110051354110051355AC25GENICpossibly homozygous118126776
10110051385110051386TC59GENICheterozygous118054284
10110051548110051549CT157GENICheterozygous118071222
10110054338110054339CT15GENIChomozygous118013231
10110051615110051616AC57GENICheterozygous118013227
10110052070110052071CA26GENIChomozygous118013229
10110052630110052631TA9GENIChomozygous118013230
10110059107110059108GT20GENIChomozygous118013232
10110077740110077741AG27GENIChomozygous118013235
10110077754110077755AG24GENIChomozygous118013236
10110077755110077756AT24GENIChomozygous118013237
10110077761110077762AC28GENIChomozygous118013238
10110077793110077794AG24GENIChomozygous118013239
10110077804110077805CT25GENIChomozygous117201122
10110077814110077815CG26GENIChomozygous118013240
10110077820110077821CG26GENIChomozygous118013241
10110077856110077857AT19GENIChomozygous116719483
10110077864110077865AT7GENIChomozygous118013242
10110077865110077866AT7GENIChomozygous118013243
10110081607110081608AG35GENIChomozygous116909835
10110091701110091702GT12GENIChomozygous116719487
10110099370110099371CT33GENIChomozygous118013247
10110099474110099475TC20GENIChomozygous118013248
10110099698110099699AT21GENIChomozygous117232664
10110054369110054370CT17GENIChomozygous117232658
10110077880110077881CG9GENIChomozygous117232660
10110054382110054383GA15GENIChomozygous117035869
10110077862110077863AT8GENIChomozygous117035871
10110100222110100223TG30GENIChomozygous116719495
10110101977110101978AG17GENICheterozygous118089338
10110101983110101984GC18GENICheterozygous118089339
10110101986110101987GA15GENICheterozygous118089341