chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1215628833215628834AG18GENIChomozygous108534758
1215633401215633402CT35GENIChomozygous120812310
1215633624215633625CG26GENIChomozygous120812312
1215637694215637695CT28GENICpossibly homozygous108534764
1215638430215638431GA28GENIChomozygous108991197
1215639315215639316GA24GENIChomozygous120812315
1215639316215639317GT25GENIChomozygous120812317
1215641220215641221TC25GENIChomozygous108534768
1215642181215642182CT29GENIChomozygous120812319
1215644264215644265GA25GENIChomozygous120812321
1215645693215645694TC29GENIChomozygous108534769
1215647181215647182AG15GENIChomozygous108991201
1215647295215647296GA22GENIChomozygous108991202
1215648350215648351CA18GENIChomozygous108534772
1215650482215650483AG21GENIChomozygous108991204
1215651196215651197GT10GENIChomozygous120812323
1215651203215651204GT16GENIChomozygous120812325
1215651461215651462GA14GENIChomozygous108991206
1215652832215652833GT34GENIChomozygous108991208
1215653364215653365AG40GENIChomozygous108991209
1215653676215653677TC33GENIChomozygous108991211
1215653730215653731GA31GENIChomozygous108991212
1215653742215653743TC30GENIChomozygous108991213
1215653746215653747AG33GENIChomozygous108991214
1215653752215653753GA34GENIChomozygous108991215
1215653754215653755GA34GENIChomozygous108991216
1215653823215653824AG25GENIChomozygous108991217
1215653957215653958AG32GENIChomozygous108991218
1215655026215655027TC30GENIChomozygous108991219
1215655079215655080AT25GENIChomozygous108534776
1215655082215655083TG26GENIChomozygous108534777
1215656092215656093TC14GENIChomozygous120812327
1215656136215656137AC8GENIChomozygous120812329
1215657250215657251CA36GENIChomozygous120812331
1215657763215657764TC28GENIChomozygous108534779
1215659387215659388CT26GENIChomozygous108534780