chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4183699852183699853AT15GENICheterozygous57026316
4183704748183704749G-1GENIChomozygous57354035
4183704749183704750T-2GENIChomozygous57354037
4183704752183704756CCCT----2GENIChomozygous57354039
4183710079183710083GTGT----19GENICheterozygous57561562
4183710081183710083GT--19GENICheterozygous57026343
4183720294183720295CCGTGT10GENIChomozygous57561590
4183725852183725853CCA7GENICheterozygous57354043
4183714218183714219TG19GENICheterozygous57858775
4183726380183726382TC--14GENICheterozygous57026378
4183726395183726396CCT16GENICheterozygous57026379
4183728159183728160C-6GENICheterozygous57026401
4183729834183729839TTTAT-----15GENICheterozygous57026415
4183729838183729839T-15GENICheterozygous57026416
4183745230183745231TC28GENIChomozygous57561618
4183745475183745477AC--20GENICpossibly homozygous57354047
4183745510183745511GGAC7GENIChomozygous57561624
4183745247183745248GT29GENIChomozygous57985950
4183745555183745556GGACAC8GENICheterozygous57985956
4183744763183744764AC30GENIChomozygous57985945
4183745225183745226AG31GENIChomozygous57985947
4183745330183745331TC38GENIChomozygous57985953
4183745615183745617AT--24GENICheterozygous57561626
4183745771183745772CT18GENIChomozygous57985959
4183745774183745775TC17GENIChomozygous57985962