chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8116730584116730585TC27GENIChomozygous116669997
8116732257116732258AG11GENIChomozygous116669999
8116734175116734176TC27GENIChomozygous116670001
8116734212116734213AG34GENIChomozygous116670003
8116736861116736862AG25GENIChomozygous116670013
8116737034116737035GA36GENIChomozygous116670015
8116737506116737507TC25GENIChomozygous116670017
8116737616116737617TG21GENIChomozygous116670019
8116737900116737901CT15GENIChomozygous116670021
8116738694116738695GA32GENIChomozygous116670023
8116740312116740313AG33GENIChomozygous116670025
8116740733116740734CT32GENIChomozygous116670027
8116741370116741371GA35GENIChomozygous116670029
8116742066116742067TC22GENIChomozygous116670031
8116742439116742440TC26GENIChomozygous116670033
8116742572116742573GA20GENIChomozygous116670035
8116742642116742643TC29GENIChomozygous116670037
8116742821116742822CT33GENIChomozygous116670039
8116743569116743570CT30GENIChomozygous116670041
8116743664116743665GA21GENIChomozygous116670043
8116744846116744847CT29GENIChomozygous116670047
8116744965116744966AT27GENIChomozygous116670049
8116745460116745461AG32GENIChomozygous116670051
8116745509116745510GA21GENIChomozygous116670053
8116746034116746035CT39GENIChomozygous116670055
8116746461116746462GA41GENIChomozygous116670057
8116746767116746768CT29GENIChomozygous116670059
8116746965116746966GA34GENIChomozygous116670061
8116747885116747886GA23GENIChomozygous116670063
8116748297116748298GA36GENIChomozygous116670065
8116748523116748524GA20GENIChomozygous116670067
8116749652116749653CT26GENIChomozygous116670069
8116749994116749995AG25GENIChomozygous116670071