chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141077246710772468GT19GENIChomozygous113338898
141077488310774884CG16GENICpossibly homozygous113338900
141077642910776430AG17GENIChomozygous113338902
141079021910790220TC11GENIChomozygous113338904
141079479110794792CG19GENIChomozygous113338906
141079688210796883AC22GENIChomozygous113338908
141079738110797382AC16GENIChomozygous113338910
141079821310798214TA24GENIChomozygous113338918
141079857310798574GC20GENIChomozygous113338920
141079883910798840TG7GENIChomozygous113338922
141079896210798963GA11GENIChomozygous113338924
141079953010799531TC10GENIChomozygous113338926
141080059310800594TC17GENIChomozygous113338928
141080089110800892AC15GENIChomozygous113338930
141080143410801435TC20GENIChomozygous113338934
141080307110803072TC30GENIChomozygous113338936
141080337510803376AG21GENIChomozygous113338938
141080444210804443TC21GENIChomozygous113338940
141080462410804625AT13GENIChomozygous113338942
141080772210807723GA12GENIChomozygous113338943
141080781810807819TC11GENIChomozygous113338944
141080853710808538CT8GENIChomozygous113338945
141080928910809290TG15GENIChomozygous113338946
141080936310809364TC11GENIChomozygous113338947
141080945710809458CT15GENIChomozygous113338948
141081231710812318GA17GENIChomozygous113338949
141081474010814741GA27GENIChomozygous113338950
141081707110817072TC7GENIChomozygous113338951
141081804010818041CA13GENIChomozygous113338952
141081864810818649CT27GENIChomozygous113338953
141082036410820365TC10GENIChomozygous113338954
141082075610820757CT10GENIChomozygous113338955
141082172610821727TA15GENIChomozygous113338956
141082373310823734TG18GENIChomozygous113338957
141082388310823884GA27GENIChomozygous113338958
141079269210792693CA14GENIChomozygous113574562
141079709810797099AG20GENIChomozygous113574563
141082673310826734CA25GENIChomozygous113338959
141082725210827253AG17GENIChomozygous113338960
141082790110827902TC15GENIChomozygous113338961