chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3100251206100251207GA51GENICheterozygous111660928
3100251416100251417AG81GENICheterozygous111976625
3100251521100251522GA90GENICheterozygous111660932
3100251700100251701AG94GENICheterozygous111660933
3100251828100251829GA60GENICheterozygous111660934
3100251858100251859GA51GENICheterozygous111976631
3100251878100251879AG46GENICheterozygous112445724
3100257449100257450TC18GENICheterozygous111660935
3100302117100302118AC23GENICheterozygous112445726
3100302121100302122CT24GENICheterozygous112445728
3100302130100302131TC27GENICheterozygous112445730
3100302134100302135CT26GENICheterozygous112445732
3100302138100302139CT24GENICheterozygous112291158
3100302140100302141CT26GENICheterozygous112291160
3100302147100302148CT31GENICheterozygous111976723
3100302156100302157GA35GENICheterozygous111976725
3100302166100302167GT35GENICheterozygous111976727
3100302170100302171TG34GENICheterozygous111976729
3100302197100302198TA28GENICheterozygous111976731
3100302201100302202AT26GENICheterozygous111976733
3100302207100302208CA29GENICheterozygous111976735
3100302213100302214GT28GENICheterozygous111976737
3100302221100302222AG27GENICheterozygous111976739
3100318138100318139TA24GENIChomozygous111660940
3100318185100318186CG14GENICpossibly homozygous111660941