chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
102928984029289841CG25GENIChomozygous116540033
102929045229290453TC22GENIChomozygous116540035
102929614429296145CG10GENIChomozygous117986110
102929640229296403CA10GENIChomozygous117986111
102929646829296469GC10GENIChomozygous117986112
102929650429296505AG14GENIChomozygous117327839
102929663329296634GC19GENIChomozygous117001353
102929663629296637AG20GENIChomozygous116540037
102929671929296720TG28GENIChomozygous116540039
102930045629300457TC9GENIChomozygous116540041
102930422529304226GT2GENIChomozygous116540043
102931632029316321AG32GENIChomozygous116540049
102931654129316542TG29GENIChomozygous116540051
102932861229328613TA30GENIChomozygous116540053
102933276429332765TA29GENICpossibly homozygous116540057
102933488629334887GC26GENIChomozygous116540059
102929678429296785GT23GENIChomozygous116751139
102932897829328979CA17GENIChomozygous116751141
102931478129314782AG24GENIChomozygous117311963
102932495329324954AC27GENICheterozygous118127979