chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
13109688208109688209CG12GENICheterozygous49987979
13109693186109693187CT13GENIChomozygous49875180
13109714961109714963AG--17GENICheterozygous49875182
13109715418109715419AAG16GENIChomozygous49875183
13109724899109724900TC10GENICheterozygous49988025
13109724907109724908TG12GENICheterozygous49988026
13109724932109724933CG22GENICheterozygous49875184
13109725009109725010TA22GENICheterozygous49875185
13109725044109725045AT9GENICheterozygous50157505
13109725054109725055TA8GENICheterozygous49988027
13109725063109725064CA9GENICheterozygous49875186
13109725065109725066TA10GENICheterozygous49875187
13109726725109726727CT--43GENICheterozygous49875188
13109726725109726726C-43GENICheterozygous49875189
13109730423109730424TC76GENICheterozygous49875190
13109730434109730435TC71GENICheterozygous49875191
13109730523109730524CT48GENICheterozygous49875192
13109731088109731089GC59GENICheterozygous49875193
13109733123109733126AAC---20GENIChomozygous50449312
13109745245109745246TC25GENICheterozygous49988080
13109745274109745275GC25GENICheterozygous49988081
13109745279109745280CT26GENICheterozygous49988082
13109745317109745318T-27GENICheterozygous49875195
13109745322109745323AT29GENICheterozygous49875196
13109745327109745328CA32GENICheterozygous49875197
13109745367109745368AG40GENICheterozygous49875198
13109751827109751828TC30GENIChomozygous49875199
13109772059109772060GA28GENICheterozygous49988155
13109772103109772104GA14GENICheterozygous49988156
13109772199109772200TTC30GENIChomozygous49875201
13109785967109785968TTGGGAGGAGGA21GENIChomozygous49875203