chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
182463610724636108GA11GENICheterozygous829960665
182463756724637568TA8GENICheterozygous829960666
182463793724637938CCGTGTGTAT10GENICheterozygous829960667
182463802324638024TG10GENICheterozygous829960668
182463841924638420AG10GENICheterozygous829960669
182463887324638874TG10GENICheterozygous829960670
182463981224639813CT7GENICheterozygous829960671
182464021824640219AG18GENICheterozygous829960672
182464052524640526AG15GENICheterozygous829960673
182464070724640708TG15GENICheterozygous829960674
182464088324640884CT12GENICheterozygous829960675
182464093724640938CT15GENICheterozygous829960676
182464096824640969TC19GENICheterozygous829960677
182464101524641016GA15GENICheterozygous829960678
182464125024641251CT10GENICheterozygous829960679
182464156924641570AG10GENICheterozygous829960680
182464220824642209GA11GENICheterozygous829960681
182464222924642230GA12GENICheterozygous829960682
182464228524642286A-9GENICheterozygous829960683
182464230024642301AG12GENICheterozygous829960684
182464293224642933AG14GENICheterozygous829960685