chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5172490279172490280AG29GENIChomozygous785359033
5172497364172497365CT16GENIChomozygous785359034
5172499346172499347GA35GENIChomozygous785359035
5172500362172500363CT29GENIChomozygous785359036
5172501606172501607AC25GENIChomozygous785359037
5172502815172502816TG21GENIChomozygous785359038
5172502911172502912AT20GENIChomozygous785359039
5172502934172502935CT21GENIChomozygous785359040
5172505791172505792GA21GENIChomozygous785359041
5172506043172506044AG16GENIChomozygous785359042
5172506077172506078CT14GENIChomozygous785359043
5172509534172509535AG26GENIChomozygous785359044
5172513051172513052AG19GENIChomozygous785359045
5172514801172514802CT19GENIChomozygous785359046
5172514993172514994AG14GENIChomozygous785359047
5172515264172515265CT19GENIChomozygous785359048
5172515860172515861CT20GENIChomozygous785359049
5172516444172516445AT15GENICheterozygous785359050
5172516910172516911AC23GENIChomozygous785359051
5172518163172518164GA30GENIChomozygous785359052
5172518373172518374TC14GENIChomozygous785359053
5172518771172518772AG7GENIChomozygous785359054
5172519862172519863AC16GENIChomozygous785359055
5172525073172525074TC22GENIChomozygous785359056
5172525452172525453TC24GENIChomozygous785359057
5172526703172526704CT11GENIChomozygous785359058
5172527818172527819GT20GENIChomozygous785359059
5172528082172528083GT16GENICpossibly homozygous785359060
5172528722172528723CT23GENIChomozygous785359061
5172531253172531254AG13GENIChomozygous785359062
5172532496172532497TC23GENIChomozygous785359063
5172538388172538389AC18GENIChomozygous785359064
5172539936172539937CT27GENIChomozygous785359065
5172542497172542498CG21GENIChomozygous785359066
5172543127172543128CT10GENIChomozygous785359067