chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5159535559159535560GA42GENIChomozygous114159779
5159536078159536079TA33GENIChomozygous114072845
5159536643159536644CT33GENIChomozygous114159780
5159536773159536774CT42GENIChomozygous114159781
5159536844159536845TC38GENIChomozygous114072848
5159536977159536978TC42GENICpossibly homozygous114159782
5159537494159537495GA28GENIChomozygous114159783
5159538052159538053GA42GENIChomozygous114072849
5159538420159538421GA52GENIChomozygous114072850
5159538443159538444TG54GENIChomozygous114072851
5159538476159538477TC44GENIChomozygous114072852
5159538742159538743AG39GENIChomozygous114072853
5159539316159539317CT83GENICheterozygous114452550
5159539343159539344GA74GENICheterozygous114452552
5159539368159539369CT73GENICheterozygous114452554
5159539400159539401GT54GENICheterozygous114452556
5159539404159539405TC55GENICheterozygous114452558
5159539419159539420TC66GENICheterozygous114452560
5159539432159539433TC73GENICheterozygous114452562
5159539446159539447AT79GENICheterozygous114452564
5159539451159539452GA83GENICheterozygous114452566
5159539696159539697CT59GENICheterozygous114452568