chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5172328487172328488GA21GENIChomozygous56365639
5172328496172328497GA21GENIChomozygous56365640
5172328969172328970AG19GENIChomozygous55842135
5172328990172328991AG17GENIChomozygous56687651
5172329346172329347AG17GENIChomozygous56195859
5172329883172329884GA32GENIChomozygous55842139
5172330034172330035AAGC19GENIChomozygous55842140
5172331443172331444AT26GENIChomozygous55842142
5172331664172331666GT--26GENIChomozygous55842144
5172332150172332151CT18GENIChomozygous56687652
5172334184172334185GGA8GENICheterozygous56687653
5172334515172334516CT28GENIChomozygous56687654
5172335178172335179GGAC18GENIChomozygous55842161
5172335459172335461CA--28GENIChomozygous56091656
5172335539172335540GGCA21GENICpossibly homozygous56687655
5172335908172335909TC29GENIChomozygous55842166
5172336411172336412AG32GENIChomozygous55842168
5172336828172336829GA25GENIChomozygous56687656
5172336972172336975GTG---25GENIChomozygous56687657
5172336975172336976GA25GENIChomozygous56687658
5172336977172336978GC24GENIChomozygous56687659