chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5172490279172490280AG40GENIChomozygous789758143
5172497364172497365CT44GENIChomozygous789758144
5172499346172499347GA29GENIChomozygous789758145
5172500362172500363CT35GENIChomozygous789758146
5172501606172501607AC26GENIChomozygous789758147
5172502815172502816TG38GENIChomozygous789758148
5172502911172502912AT33GENIChomozygous789758149
5172502934172502935CT30GENIChomozygous789758150
5172505791172505792GA29GENIChomozygous789758151
5172506043172506044AG24GENIChomozygous789758152
5172506077172506078CT34GENIChomozygous789758153
5172509534172509535AG19GENICpossibly homozygous789758154
5172513051172513052AG38GENIChomozygous789758155
5172514801172514802CT30GENIChomozygous789758156
5172514993172514994AG42GENIChomozygous789758157
5172515264172515265CT24GENIChomozygous789758158
5172515860172515861CT25GENIChomozygous789758159
5172516444172516445AT67GENICheterozygous789758160
5172516910172516911AC22GENIChomozygous789758161
5172518163172518164GA39GENIChomozygous789758162
5172518373172518374TC26GENIChomozygous789758163
5172518771172518772AG13GENIChomozygous789758164
5172519862172519863AC33GENIChomozygous789758165
5172525073172525074TC36GENIChomozygous789758166
5172525452172525453TC26GENIChomozygous789758167
5172526703172526704CT23GENIChomozygous789758168
5172527818172527819GT24GENIChomozygous789758169
5172528082172528083GT37GENIChomozygous789758170
5172528722172528723CT37GENIChomozygous789758171
5172531253172531254AG28GENIChomozygous789758172
5172532496172532497TC40GENIChomozygous789758173
5172538388172538389AC40GENIChomozygous789758174
5172539936172539937CT24GENIChomozygous789758175
5172542497172542498CG28GENIChomozygous789758176
5172543127172543128CT21GENIChomozygous789758177