chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1045497434549744TC32GENICheterozygous51307798
1045573834557384GA16GENICheterozygous51307852
1045573864557387CT16GENICheterozygous51307853
1046915194691520CG26GENICheterozygous51609300
1046916494691650CG46GENICheterozygous51609301
1046917384691739AG46GENICheterozygous51609302
1046917414691742AC47GENICheterozygous51308362
1046938684693869CT25GENICheterozygous51609312
1046939084693909AG21GENICheterozygous51609313
1046948624694863GA23GENICheterozygous51609320
1047109634710964AC45GENICheterozygous51609372
1047435584743559AG13GENICheterozygous51308508
1047654304765431GA33GENICheterozygous51609452
1047846564784657CT21GENICheterozygous51609507
1047980664798067CT29GENICheterozygous51609577
1047981554798156GT33GENICheterozygous51609578
1047984514798452AG25GENICheterozygous51609579
1048007614800762CT23GENICheterozygous51609589
1048007734800774TC18GENICheterozygous51308701
1048207904820791TC25GENICheterozygous51308778
1048231384823139GGAGTCTCTC14GENICheterozygous51609638
1048287834828784TC20GENICheterozygous51308811
1048288454828846CA11GENICheterozygous51308812
1048339234833924CT90GENICheterozygous51308843
1048341094834110AG38GENICheterozygous51609648
1048344434834444TC19GENICheterozygous51308845
1048345894834591TT--38GENICheterozygous51308846
1048443364844337GA39GENICheterozygous51308890
1048443854844386GA27GENICheterozygous51609664
1048517684851769CT53GENICheterozygous51609696
1048542934854294GA19GENICheterozygous51609710
1048575334857534TC28GENICheterozygous51609735
1048646854864686TC21GENICheterozygous51308929
1048647494864750GA24GENICheterozygous51308931
1049047154904716CA42GENICheterozygous51309086
1049112664911267CT33GENICheterozygous51609806
1049351294935130AG42GENICheterozygous51609842
1049370464937047TC34GENICheterozygous51309205
1049371474937148GA42GENICheterozygous51609843
1049373554937356GGC14GENICheterozygous51609844
1049407464940747AT23GENICheterozygous51309211