chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
64070091040700911GC15GENICheterozygous880140062
64070110940701110GC18GENIChomozygous880140063
64070167240701673GA12GENIChomozygous880140064
64070177840701779AG22GENIChomozygous880140065
64070202040702021GT17GENIChomozygous880140066
64070221440702215AG8GENIChomozygous880140067
64070222940702230AC5GENIChomozygous880140068
64070227740702278GC14GENIChomozygous880140069
64070229840702299AT15GENIChomozygous880140070
64070257740702578GA14GENIChomozygous880140071
64070268040702681CT20GENIChomozygous880140072
64070310940703110AG12GENIChomozygous880140073
64070313740703138TC13GENIChomozygous880140074
64070335840703359AG11GENIChomozygous880140075
64070400940704010CA21GENIChomozygous880140076
64070618040706181CA30GENIChomozygous880140077
64070641040706411GT12GENIChomozygous880140078
64070747540707476GT13GENIChomozygous880140079
64070774040707741GC9GENIChomozygous880140080
64070799540707996GA6GENIChomozygous880140081
64070808740708088CA3GENICheterozygous880140082
64070870140708702CT15GENIChomozygous880140083
64070879140708792AG20GENIChomozygous880140084
64070914340709144TA8GENIChomozygous880140085
64070915340709154TG9GENIChomozygous880140086
64070943240709433TC18GENIChomozygous880140087
64070947140709472TA12GENIChomozygous880140088
64070985340709854TA8GENIChomozygous880140089
64070985440709855GC8GENIChomozygous880140090
64070988040709881GA10GENIChomozygous880140091
64071041340710414TC21GENIChomozygous880140092
64071066740710668GA11GENIChomozygous880140093
64071076740710768CT5GENIChomozygous880140094
64071079940710800AG8GENIChomozygous880140095
64071250040712501TA21GENIChomozygous880140096
64071331540713316TC11GENIChomozygous880140097
64071333840713339GA17GENIChomozygous880140098