chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
116037200760372008TG25GENIChomozygous116155021
116037216260372163TA24GENIChomozygous116155023
116037229060372291TA34GENIChomozygous116155025
116037268560372686TG25GENIChomozygous116155027
116037273160372732TC25GENIChomozygous116155029
116037302660373027CT21GENIChomozygous116155031
116037342860373429TC24GENIChomozygous115877587
116037425760374258GA33GENIChomozygous115877589
116037491660374917TC33GENIChomozygous116155033
116037547760375478AG32GENIChomozygous116155035
116037617460376175AG41GENIChomozygous115877591
116037622260376223TA40GENIChomozygous115877593
116037755660377557CT34GENIChomozygous116155037
116037794860377949AC30GENIChomozygous116155039
116037916960379170AG26GENIChomozygous115877597
116037993060379931GA25GENIChomozygous116155041
116038073660380737CA22GENIChomozygous116155043
116038224960382250AG40GENIChomozygous115976717
116038391860383919CT32GENIChomozygous116155045
116038487560384876TC26GENIChomozygous115877624
116038595560385956GA30GENIChomozygous116155047
116038769260387693TC34GENIChomozygous115877634
116038738660387387CT34GENIChomozygous115877630
116038833060388331GA28GENIChomozygous116155049
116039099260390993TC37GENIChomozygous115877638
116039395360393954AC34GENIChomozygous116155051
116039414660394147TC14GENIChomozygous115877644
116039427060394271CG27GENIChomozygous116155053
116039428060394281CG33GENIChomozygous116155055
116039437760394378TC35GENIChomozygous116155057
116039443760394438AC48GENIChomozygous116155059
116039557760395578AG23GENIChomozygous115877650
116039620860396209GT39GENIChomozygous116155061
116039624160396242GA35GENIChomozygous115877652
116039624560396246CA34GENIChomozygous116155063
116039675760396758CA32GENIChomozygous116155065
116039695960396960GT33GENIChomozygous116155067
116039701260397013GC34GENIChomozygous116155069
116039735860397359AG21GENIChomozygous116155071
116039745560397456AG16GENIChomozygous116155073
116039837660398377AG33GENIChomozygous116155075