chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106377610663776107GC9GENIChomozygous955797312
106377622363776224AG29GENIChomozygous955797313
106378025263780253GT42GENIChomozygous955797314
106378207463782075TC35GENIChomozygous955797315
106378294663782947CT34GENIChomozygous955797316
106378403763784038CG44GENIChomozygous955797317
106378485563784856GA47GENIChomozygous955797318
106378928963789290TC38GENIChomozygous955797319
106378943963789440GT34GENICpossibly homozygous955797320
106379062063790621AC28GENIChomozygous955797321
106379067163790672TC35GENIChomozygous955797322
106379279063792791CT33GENIChomozygous955797323
106379466163794662GT27GENIChomozygous955797324
106379483063794831TG35GENIChomozygous955797325
106379501463795015TC34GENIChomozygous955797326