chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1165483149165483150AT27GENIChomozygous108353925
1165483225165483226CA26GENIChomozygous108353927
1165483620165483621CT12GENIChomozygous108353929
1165483651165483652CT17GENIChomozygous108353931
1165483673165483674AG20GENIChomozygous109436129
1165483687165483688GT20GENIChomozygous108353933
1165483805165483806GA20GENIChomozygous108353935
1165484070165484071AG26GENIChomozygous108353937
1165484364165484368AGTC20GENIChomozygous127452831
1165484797165484798AG17GENIChomozygous108353939
1165484854165484855CT19GENIChomozygous108353941
1165484879165484880TC19GENIChomozygous108353943
1165485265165485266CT14GENIChomozygous108353945
1165485329165485330CT9GENIChomozygous108353947
1165485421165485422CG17GENIChomozygous108353949
1165485597165485598AG24GENIChomozygous108353951
1165486329165486330CA26GENIChomozygous108353953
1165486745165486746AG29GENIChomozygous108353955
1165487305165487307AT10GENIChomozygous127452832
1165488872165488873CT21GENIChomozygous109436131
1165488963165488964AG30GENIChomozygous108353959
1165490953165490954CT23GENIChomozygous108353960
1165492011165492012GA19GENIChomozygous108353964
1165492396165492396AG7GENIChomozygous133801015
1165492587165492588AG20GENIChomozygous108353968
1165493703165493704TC21GENIChomozygous108353972
1165495186165495187CT31GENIChomozygous109436135
1165495417165495418AG21GENIChomozygous108353974
1165495487165495487G21GENIChomozygous133801016
1165495861165495862AG25GENIChomozygous108954382