chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1165483149165483150AT21GENIChomozygous108353925
1165483225165483226CA20GENIChomozygous108353927
1165483620165483621CT20GENIChomozygous108353929
1165483651165483652CT14GENIChomozygous108353931
1165483673165483674AG12GENIChomozygous109436129
1165483687165483688GT11GENIChomozygous108353933
1165483805165483806GA15GENIChomozygous108353935
1165484070165484071AG16GENIChomozygous108353937
1165484797165484798AG19GENIChomozygous108353939
1165484854165484855CT20GENIChomozygous108353941
1165484879165484880TC17GENIChomozygous108353943
1165485421165485422CG29GENIChomozygous108353949
1165485597165485598AG20GENIChomozygous108353951
1165486329165486330CA18GENIChomozygous108353953
1165486745165486746AG23GENIChomozygous108353955
1165488872165488873CT21GENIChomozygous109436131
1165488963165488964AG20GENIChomozygous108353959
1165490953165490954CT17GENIChomozygous108353960
1165492011165492012GA24GENIChomozygous108353964
1165492587165492588AG20GENIChomozygous108353968
1165493703165493704TC20GENIChomozygous108353972
1165495186165495187CT16GENIChomozygous109436135
1165495417165495418AG17GENIChomozygous108353974
1165495861165495862AG27GENIChomozygous108954382