chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
184060675640606757CT15GENICpossibly homozygous564843069
184060684840606849AT14GENICheterozygous564843070
184060730840607309AG16GENIChomozygous564843071
184060747840607481CAT---5GENIChomozygous707978388
184060836840608369TC18GENIChomozygous564843072
184060913440609135AG7GENIChomozygous564843073
184060915740609158GT8GENICheterozygous564843074
184060922040609221AG2GENIChomozygous564843075
184060963040609631AG2GENIChomozygous564843076
184061158040611581GC1GENIChomozygous564843077
184061194540611946AG7GENIChomozygous562252796
184061304940613050CA14GENIChomozygous564843078
184061710140617102GA4GENIChomozygous564843079
184061764740617648CT6GENIChomozygous564843080
184061773440617735TC12GENICheterozygous564843081
184061774840617749GT9GENICpossibly homozygous564843082
184061777840617779AG7GENICpossibly homozygous564843083
184061833040618331GA11GENICpossibly homozygous564843084
184061904140619042AG13GENICpossibly homozygous564843085
184061928940619290AG11GENIChomozygous564843086
184061989240619893GA15GENIChomozygous564843087
184062017040620171AG22GENICpossibly homozygous564843088
184062283840622839AG16GENIChomozygous564843089
184062418440624185GA24GENICpossibly homozygous564843090
184062465840624659GC18GENICpossibly homozygous564843091
184062514940625150AG18GENIChomozygous564843092
184062646740626468AC12GENIChomozygous564843093
184062819840628199GA12GENIChomozygous562252797
184062853540628536CT7GENIChomozygous564843094
184062860140628602CT8GENIChomozygous564843095
184063111140631112T-8GENIChomozygous707978389
184063123440631235GA7GENICpossibly homozygous564843096
184063333540633336AC14GENICpossibly homozygous564843097