chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4152091907152091908CT39GENICheterozygous57520620
4152092112152092113CT41GENICheterozygous58159925
4152092162152092163AG47GENICheterozygous58159927
4152092756152092757GC36INTERGENICheterozygous58159929
4152110097152110098A-46GENICheterozygous58160007
4152161034152161035TG59GENICheterozygous58160054
4152161424152161425TC51GENICheterozygous58160060
4152161472152161473AAT61GENICheterozygous58160062
4152249897152249898GT53GENICheterozygous58087015
4152250183152250184AG88GENICheterozygous56985048
4152250219152250220CT70GENICheterozygous56985049
4152250361152250362GA28INTERGENICheterozygous58160180
4152339882152339883GA38GENICheterozygous56985524
4152340117152340118TG69GENICheterozygous56985525
4152343929152343930CT57GENICheterozygous56985547
4152344174152344175AAT62GENICheterozygous56985548
4152344486152344487AG139GENICheterozygous56985549
4152344573152344574AG79GENICheterozygous56985550
4152344907152344908CT22INTERGENICheterozygous56985552
4152344908152344909CG23INTERGENICheterozygous56985553
4152344919152344920AT24INTERGENICheterozygous56985554