chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5172328487172328488GA10GENIChomozygous56365639
5172328496172328497GA12GENIChomozygous56365640
5172328969172328970AG14GENIChomozygous55842135
5172328990172328991AG14GENICpossibly homozygous56687651
5172329346172329347AG11GENIChomozygous56195859
5172329883172329884GA11GENIChomozygous55842139
5172330034172330035AAGC10GENIChomozygous55842140
5172331443172331444AT11GENICheterozygous55842142
5172331664172331666GT--5GENIChomozygous55842144
5172332150172332151CT12GENIChomozygous56687652
5172334515172334516CT5GENIChomozygous56687654
5172335459172335461CA--1GENIChomozygous56091656
5172335908172335909TC10GENICpossibly homozygous55842166
5172336828172336829GA16GENIChomozygous56687656