chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
9113206097113206098T25GENICheterozygous403273311
9113206097113206098TG25GENICheterozygous403273312
9113206099113206100TG25GENICheterozygous154617910
9113206099113206100T25GENICheterozygous403273313
9113206103113206104TG26GENICheterozygous144077069
9113221074113221075TC22GENIChomozygous142194148
9113222412113222413GA48GENIChomozygous138660374
9113226503113226504AG39GENIChomozygous138660375
9113228082113228083CA25GENIChomozygous142194149
9113229180113229181AT40GENIChomozygous142194150
9113222661113222662A44GENICpossibly homozygous142123025
9113231606113231607AG50GENIChomozygous138660376
9113241310113241311AG45GENIChomozygous142194151
9113246092113246093CG34GENIChomozygous142194152
9113246870113246871GT11GENIChomozygous138660380
9113233630113233630T47GENICpossibly homozygous138481216
9113237750113237750T43GENIChomozygous138481217
9113227705113227706T22GENIChomozygous142123026
9113230888113230888G4GENICheterozygous145147310
9113247202113247203AT31GENIChomozygous403273318
9113248961113248962GA47GENIChomozygous142194153
9113250856113250856CG13GENICheterozygous142123029
9113251578113251579GA47GENIChomozygous142194154
9113254852113254853CT38GENIChomozygous138660382
9113263077113263078A34GENIChomozygous138481218
9113263799113263799ATACTGGACAAAA43GENIChomozygous138481219
9113265326113265327AG41GENIChomozygous138660383