chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
162486311324863114CCGT2GENIChomozygous707915261
162486313224863133TA5GENIChomozygous564344736
162486320324863204TA16GENICpossibly homozygous563498345
162486376124863762GA11GENICpossibly homozygous564344737
162486389124863892GC8GENIChomozygous563498346
162486399024863991GGT5GENICheterozygous707915262
162486527524865276A-12GENIChomozygous707915263
162486561624865617CT2GENIChomozygous563498347
162486670024866701TC10GENIChomozygous564344738
162486680224866803CT18GENIChomozygous564344739
162486702724867028CCT14GENICpossibly homozygous707915264
162486775724867758AG23GENIChomozygous564344740
162486855024868551CT14GENIChomozygous563498348
162486918724869188CT10GENIChomozygous564344741
162486920124869202GA12GENIChomozygous564344742
162486940724869408TA15GENICheterozygous563498349
162486964924869653TAAG----9GENIChomozygous707915265
162486971724869718GC8GENIChomozygous564344743
162486974824869749A-5GENIChomozygous707915266
162487027424870275CG24GENIChomozygous564344744
162487135524871356CG10GENIChomozygous563498350
162487169924871700CT8GENIChomozygous564344745
162487173724871738CA4GENIChomozygous564344746