chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5172490279172490280AG40GENIChomozygous941138005
5172497364172497365CT41GENIChomozygous941138006
5172499346172499347GA29GENIChomozygous941138007
5172500362172500363CT35GENIChomozygous941138008
5172501606172501607AC26GENIChomozygous941138009
5172502815172502816TG37GENIChomozygous941138010
5172502911172502912AT33GENIChomozygous941138011
5172502934172502935CT30GENIChomozygous941138012
5172505791172505792GA29GENIChomozygous941138013
5172506043172506044AG24GENIChomozygous941138014
5172506077172506078CT34GENIChomozygous941138015
5172513051172513052AG38GENIChomozygous941138016
5172514801172514802CT29GENIChomozygous941138017
5172515264172515265CT24GENIChomozygous941138018
5172515860172515861CT25GENIChomozygous941138019
5172516910172516911AC22GENIChomozygous941138020
5172518163172518164GA39GENIChomozygous941138021
5172518373172518374TC26GENIChomozygous941138022
5172519862172519863AC33GENIChomozygous941138023
5172525073172525074TC36GENIChomozygous941138024
5172525452172525453TC26GENIChomozygous941138025
5172526703172526704CT23GENIChomozygous941138026
5172527818172527819GT24GENIChomozygous941138027
5172528082172528083GT36GENIChomozygous941138028
5172528722172528723CT37INTERGENIChomozygous941138029
5172531253172531254AG28INTERGENIChomozygous941138030
5172532496172532497TC39INTERGENIChomozygous941138031
5172535324172535325CA4INTERGENIChomozygous941138032
5172538388172538389AC40INTERGENIChomozygous941138033
5172539936172539937CT23INTERGENIChomozygous941138034
5172542497172542498CG28INTERGENIChomozygous941138035
5172543127172543128CT21INTERGENIChomozygous941138036