chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
95257215752572158GA34GENIChomozygous634981950
95257223752572238TC27GENIChomozygous634981951
95257285452572855GT22GENIChomozygous634981952
95257290352572904AG24GENIChomozygous634981953
95257291752572918GT26GENIChomozygous634981954
95257312052573121AG21GENIChomozygous634981955
95257317852573179TC20GENIChomozygous634981956
95257320852573209AT21GENIChomozygous634981957
95257323452573235CA17GENIChomozygous634981958
95257334052573341TA28GENIChomozygous634981959
95257362752573628AG26GENIChomozygous634981960
95257373052573733TAG---19GENIChomozygous747784200
95257378952573790TA21GENIChomozygous634981961
95257419252574193AG29GENIChomozygous634981962
95257447552574476GA20GENICpossibly homozygous634981963
95257448952574490CT19GENIChomozygous634981964
95257469652574697TC23GENIChomozygous634981965
95257473752574738TC25GENIChomozygous634981966
95257512052575121GA41GENIChomozygous634981967
95257545052575451AG29GENIChomozygous634981968
95257567152575672AG13GENIChomozygous634981969
95257626852576269CA21GENIChomozygous634981970
95257628052576281TG17GENIChomozygous634981971
95257632152576322GC15GENIChomozygous634981972
95257651352576514CCT23GENIChomozygous747784201
95257661052576611TC20GENIChomozygous634981973
95257665052576651TA23GENIChomozygous634981974
95257683152576832AG25GENIChomozygous634981975
95257701252577013AT33GENIChomozygous634981976
95257741352577414CT33GENIChomozygous634981977
95257750252577503AT30GENIChomozygous634981978
95257762252577623AG32GENIChomozygous634981979
95257765652577657AG30GENIChomozygous634981980