chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
154145999841459999AG28GENIChomozygous112490375
154146005041460051CA25GENIChomozygous112490377
154146005241460053CA24GENIChomozygous112490379
154146007241460073AG22GENIChomozygous112490381
154146008041460081GA19GENIChomozygous112490383
154146009141460092GA21GENIChomozygous112490385
154146012241460123GT25GENIChomozygous112490387
154146015541460156GC21GENIChomozygous112490389
154147565741475658AG26GENICheterozygous112808546
154148196241481963TC19GENIChomozygous112808548
154148198341481984TC19GENIChomozygous112672877
154148199041481991GC17GENIChomozygous112672879
154148873041488731GT20GENIChomozygous112808550
154148875641488757GC19GENIChomozygous112808552
154148876741488768CA20GENIChomozygous112490671
154148879841488799AT19GENIChomozygous112490673