chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71162739611627397AC21GENIChomozygous53788708
71162748711627488GA11GENIChomozygous53788709
71162852311628524TC9GENIChomozygous53788710
71162963411629635AG17GENIChomozygous53788711
71163003311630034AC9GENIChomozygous54181608
71163003911630040AC9GENIChomozygous53788713
71163018911630190AAAAAAAAAAAAAAAAAAAAAGAACC8GENICpossibly homozygous54954467
71163078811630789CT7GENIChomozygous53788715
71163182711631828CCT16GENICpossibly homozygous53788716
71163183811631839CT20GENIChomozygous54181610
71163258811632589GA21GENIChomozygous53788718
71163341611633417TC15GENIChomozygous53788719
71163351911633520CA24GENIChomozygous53788720
71163352511633526AG22GENIChomozygous53788721
71163353811633539AC22GENIChomozygous53788722
71163493111634932TC11GENIChomozygous53788723
71163581511635816AT19GENIChomozygous53788724
71163724911637250T-13GENIChomozygous54181611
71163743311637434AG15GENIChomozygous53788725
71163923211639233TC13GENIChomozygous53788726
71163949911639500CT23GENIChomozygous53788727
71163968911639690GA12GENIChomozygous53788728
71163987311639874AAT20GENIChomozygous53788729
71164090611640907TC36GENIChomozygous54884856
71164090711640908CA37GENIChomozygous54181612
71164275011642751AG21GENIChomozygous53788731
71164349411643495AG13GENIChomozygous53788732
71164382611643827TTCTGG19GENIChomozygous53788733
71164383511643836CT19GENIChomozygous53788734
71164403211644033TC14GENIChomozygous53788735
71164448411644485TG20GENIChomozygous53788736
71164452411644525TC12GENIChomozygous53788737
71164475611644757TC8GENIChomozygous53788738
71164563611645637CT4GENIChomozygous53788739