chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71162739611627397AC33GENIChomozygous53788708
71162748711627488GA20GENIChomozygous53788709
71162852311628524TC16GENIChomozygous53788710
71162963411629635AG27GENIChomozygous53788711
71163003311630034AC9GENIChomozygous54181608
71163003911630040AC10GENIChomozygous53788713
71163018911630190AAAAAAAAAAAAAAAAAAAAAGAACC21GENICpossibly homozygous54954467
71163078811630789CT24GENIChomozygous53788715
71163182711631828CCT16GENIChomozygous53788716
71163183811631839CT19GENIChomozygous54181610
71163258811632589GA21GENIChomozygous53788718
71163341611633417TC20GENIChomozygous53788719
71163351911633520CA20GENIChomozygous53788720
71163352511633526AG20GENIChomozygous53788721
71163353811633539AC21GENIChomozygous53788722
71163493111634932TC31GENIChomozygous53788723
71163581511635816AT29GENIChomozygous53788724
71163724911637250T-18GENICpossibly homozygous54181611
71163743311637434AG27GENIChomozygous53788725
71163923211639233TC22GENIChomozygous53788726
71163949911639500CT29GENIChomozygous53788727
71163968911639690GA28GENIChomozygous53788728
71163987311639874AAT33GENIChomozygous53788729
71164090611640907TC33GENIChomozygous54884856
71164090711640908CA33GENIChomozygous54181612
71164275011642751AG32GENIChomozygous53788731
71164349411643495AG21GENIChomozygous53788732
71164382611643827TTCTGG22GENIChomozygous53788733
71164383511643836CT19GENIChomozygous53788734
71164403211644033TC17GENIChomozygous53788735
71164448411644485TG24GENICpossibly homozygous53788736
71164452411644525TC24GENIChomozygous53788737
71164475611644757TC11GENIChomozygous53788738
71164563611645637CT9GENIChomozygous53788739