chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5172490279172490280AG60GENIChomozygous775488157
5172497364172497365CT48GENICpossibly homozygous775488158
5172499346172499347GA51GENIChomozygous775488159
5172500362172500363CT53GENIChomozygous775488160
5172501606172501607AC34GENICpossibly homozygous775488161
5172502815172502816TG46GENIChomozygous775488162
5172502911172502912AT46GENIChomozygous775488163
5172502934172502935CT51GENIChomozygous775488164
5172505791172505792GA58GENIChomozygous775488165
5172506043172506044AG32GENIChomozygous775488166
5172506077172506078CT32GENIChomozygous775488167
5172509534172509535AG25GENIChomozygous775488168
5172513051172513052AG41GENIChomozygous775488169
5172514801172514802CT38GENIChomozygous775488170
5172514993172514994AG37GENIChomozygous775488171
5172515264172515265CT40GENIChomozygous775488172
5172515860172515861CT57GENIChomozygous775488173
5172516444172516445AT37GENICheterozygous775488174
5172516910172516911AC47GENIChomozygous775488175
5172518163172518164GA49GENIChomozygous775488176
5172518373172518374TC45GENIChomozygous775488177
5172518771172518772AG24GENICpossibly homozygous775488178
5172519862172519863AC36GENICpossibly homozygous775488179
5172525073172525074TC47GENIChomozygous775488180
5172525452172525453TC54GENIChomozygous775488181
5172526703172526704CT22GENIChomozygous775488182
5172527818172527819GT35GENIChomozygous775488183
5172528082172528083GT32GENIChomozygous775488184
5172528722172528723CT34GENIChomozygous775488185
5172531253172531254AG44GENIChomozygous775488186
5172532496172532497TC42GENIChomozygous775488187
5172538388172538389AC53GENIChomozygous775488188
5172539936172539937CT37GENIChomozygous775488189
5172542497172542498CG47GENIChomozygous775488190
5172543127172543128CT23GENIChomozygous775488191