chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109021144190211442GA66GENIChomozygous68165194
109021235690212357GA64GENICpossibly homozygous68165197
109021491290214913TA44GENIChomozygous68165200
109021515490215155GA39GENIChomozygous68165203
109021696190216962TC51GENIChomozygous68165206
109021990690219907CA39GENIChomozygous68165210
109021993590219936CG29GENIChomozygous68165213
109021994090219941TG28GENIChomozygous68165216
109021994590219946CA24GENIChomozygous68165219
109021995190219952CA22GENIChomozygous68165222
109022031190220312GA53GENIChomozygous68165225
109022155490221555AC54GENIChomozygous68165228
109022178290221783AG48GENIChomozygous68165231
109022243490222435TC43GENIChomozygous68165234
109022272390222724CT63GENIChomozygous68165237
109022302390223024AG58GENIChomozygous68165240
109022353190223532CT40GENIChomozygous68165243
109022603890226039TG30GENICheterozygous68165253
109022416190224162CT54GENIChomozygous68165246
109022417390224174AG49GENIChomozygous68165249
109022608090226081AG27GENIChomozygous68165256
109022758490227585TC44GENIChomozygous68165259
109022775490227755TG47GENICpossibly homozygous68165262
109022903390229034AG57GENIChomozygous68165265
109022912790229128AG67GENIChomozygous68165268
109023152190231522GC65GENIChomozygous68165271
109023180590231806GC61GENIChomozygous68165274
109023304490233045TC41GENIChomozygous68165277
109023369890233699AT33GENICheterozygous68165280
109023370790233708GC35GENICpossibly homozygous68165283
109023463690234637AG47GENIChomozygous68165286
109023468590234686AG64GENIChomozygous68165289
109023634090236341CT63GENIChomozygous68165292