chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
48708947387089474TC42GENIChomozygous112767369
48709208887092089GA21GENIChomozygous112767371
48709245387092454CA9GENIChomozygous112767375
48709317787093178AG23GENIChomozygous113517790
48709339387093394CT25GENIChomozygous113280962
48709436487094365CT29GENIChomozygous113517792
48709575187095752CT11GENIChomozygous113517794
48709731987097320GT28GENIChomozygous112767379
48709812887098129CA11GENIChomozygous112767381
48709831187098312AG16GENIChomozygous112767383
48709864787098648AC17GENIChomozygous112767385
48709879687098797CT20GENIChomozygous113280964
48709913187099132AT17GENIChomozygous113517796
48709963687099637GA11GENIChomozygous112767387
48709974487099745AC20GENIChomozygous113280965
48709992587099926AG17GENICheterozygous112767389
48709995787099958CA15GENIChomozygous112767391
48710084987100850CA15GENIChomozygous112767393
48710156787101568GC24GENIChomozygous113280966
48710196887101969TC11GENIChomozygous112767397
48710263287102633CA13GENIChomozygous113130247
48710351287103513TC16GENIChomozygous112767401
48710375787103758TC18GENIChomozygous112767403
48710577187105772TG19GENIChomozygous112767409
48710589687105897TC14GENIChomozygous113280968
48710607487106075GA17GENIChomozygous112767411
48710614087106141TC11GENIChomozygous113280969
48710663387106634CT33GENIChomozygous112767415
48710668687106687AT24GENIChomozygous112767417
48710686087106861GA30GENIChomozygous112767419
48710861787108618TA30GENIChomozygous113280971
48711116587111166AG4GENIChomozygous112767425