chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1171539112171539113TG12GENIChomozygous120679017
1171539336171539337TC18GENIChomozygous120679019
1171545349171545350GC39GENIChomozygous108378215
1171546808171546809TC15GENIChomozygous120679021
1171546974171546975AT20GENIChomozygous108378219
1171549137171549138GA26GENICpossibly homozygous108378221
1171549564171549565AG37GENIChomozygous108378223
1171549976171549977AG33GENIChomozygous108378225
1171550738171550739CG21GENIChomozygous120679023
1171552696171552697TG13GENIChomozygous120679025
1171552697171552698AG14GENIChomozygous120679027
1171553708171553709GA20GENIChomozygous120679029
1171554617171554618TA20GENIChomozygous120679031
1171557058171557059TA19GENIChomozygous109167904
1171557720171557721TC26GENIChomozygous120679033
1171561704171561705CA24GENIChomozygous120679035
1171561769171561770CT23GENIChomozygous120679037
1171561779171561780AG23GENIChomozygous109167920
1171562998171562999AG22GENIChomozygous120679039
1171563071171563072TC19GENIChomozygous108378240
1171564163171564164GA26GENIChomozygous120679041
1171564686171564687AG28GENICpossibly homozygous120679043
1171564691171564692TG28GENICpossibly homozygous120679046
1171564983171564984AG17GENIChomozygous120679048
1171565005171565006GC23GENIChomozygous120679050
1171565121171565122AC25GENIChomozygous109167928
1171565675171565676CT24GENIChomozygous109167930