chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5172328487172328488GA23GENIChomozygous56365639
5172328496172328497GA26GENIChomozygous56365640
5172328969172328970AG18GENIChomozygous55842135
5172328990172328991AG18GENIChomozygous56687651
5172329346172329347AG19GENIChomozygous56195859
5172329883172329884GA18GENIChomozygous55842139
5172330034172330035AAGC30GENIChomozygous55842140
5172331443172331444AT22GENIChomozygous55842142
5172331664172331666GT--22GENIChomozygous55842144
5172332150172332151CT28GENIChomozygous56687652
5172334184172334185GGA6GENICheterozygous56687653
5172334201172334202G-17GENICheterozygous56676114
5172334515172334516CT28GENIChomozygous56687654
5172335178172335179GGAC18GENICheterozygous55842161
5172335459172335461CA--20GENIChomozygous56091656
5172335539172335540GGCA9GENIChomozygous56687655
5172335908172335909TC20GENIChomozygous55842166
5172336411172336412AG14GENIChomozygous55842168
5172336828172336829GA24GENIChomozygous56687656
5172336972172336975GTG---19GENIChomozygous56687657
5172336975172336976GA17GENIChomozygous56687658
5172336977172336978GC15GENIChomozygous56687659