chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
162486311324863114CCGT20GENIChomozygous750810932
162486313224863133TA25GENIChomozygous639676319
162486320324863204TA26GENIChomozygous639676320
162486376124863762GA9GENIChomozygous639676321
162486389124863892GC15GENIChomozygous639676322
162486399024863991GGT13GENIChomozygous750810933
162486527524865276A-34GENIChomozygous750810934
162486561624865617CT20GENIChomozygous639676323
162486564424865664TCTTTCTTTCTTTCTTTCTT--------------------17GENIChomozygous750810936
162486670024866701TC15GENIChomozygous639676324
162486680224866803CT14GENICpossibly homozygous639676325
162486702724867028CCT29GENIChomozygous750810938
162486775724867758AG24GENIChomozygous639676326
162486855024868551CT29GENIChomozygous639676327
162486918724869188CT11GENIChomozygous639676328
162486920124869202GA10GENIChomozygous639676329
162486940724869408TA16GENIChomozygous639676330
162486964924869653TAAG----11GENIChomozygous750810939
162486971724869718GC14GENIChomozygous639676331
162486974824869749A-12GENIChomozygous750810940
162487027424870275CG17GENIChomozygous639676332
162487135524871356CG6GENIChomozygous639676333
162487138124871382GGT5GENICheterozygous750810941
162487154224871543TC1GENIChomozygous639676334
162487154424871545CG1GENIChomozygous639676335
162487156524871566TA1GENIChomozygous639676336
162487169924871700CT12GENIChomozygous639676337
162487173724871738CA13GENICheterozygous639676338