chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
154146005041460051CA29GENIChomozygous112490377
154146005241460053CA29GENIChomozygous112490379
154146007241460073AG27GENIChomozygous112490381
154146008041460081GA28GENIChomozygous112490383
154146009141460092GA27GENIChomozygous112490385
154146012241460123GT25GENIChomozygous112490387
154146015541460156GC23GENIChomozygous112490389
154148196241481963TC24GENIChomozygous112808548
154148198341481984TC21GENIChomozygous112672877
154148199041481991GC21GENIChomozygous112672879
154148869241488693CA18GENIChomozygous112490669
154148873041488731GT27GENIChomozygous112808550
154148875641488757GC23GENIChomozygous112808552
154148876741488768CA24GENIChomozygous112490671
154148879841488799AT25GENIChomozygous112490673