chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
76346821463468215CT14GENIChomozygous126526767
76346822963468230TG17GENIChomozygous126526769
76346883763468838CT17GENIChomozygous126526771
76346905463469055TA4GENIChomozygous126597975
76346989163469892TC6GENIChomozygous126526773
76347079263470793CT21GENIChomozygous126526775
76347123663471237GA23GENIChomozygous126526777
76347188363471884CT19GENIChomozygous126526779
76347576263475763GA25GENIChomozygous126526781
76347628863476289CT11GENIChomozygous126526783
76347633563476336CT12GENIChomozygous126526785
76347654463476545GA14GENIChomozygous126577735
76347834663478347AG22GENIChomozygous126526787
76347909563479096AG17GENIChomozygous126526789
76347913963479140TC18GENIChomozygous126526791
76347989363479894TC18GENIChomozygous126526793
76347993863479939AG14GENIChomozygous126526795
76348043163480432TC17GENIChomozygous126526797
76348215763482158CT7GENIChomozygous126526799
76348245063482451GA27GENIChomozygous126526801
76348284363482844TC14GENIChomozygous126526803
76348318663483187GA11GENICheterozygous126526805
76348318663483187GA11GENICheterozygous126526805
76348318963483190GA13GENIChomozygous126526807
76348440963484410CT17GENIChomozygous126526809
76348736763487368GA22GENIChomozygous126526815
76348809763488098AG26GENIChomozygous126526817
76348815363488154GA17GENIChomozygous126526819
76349097863490979TC13GENIChomozygous126526823
76349114763491148AG18GENIChomozygous126526825
76349151063491511GA29GENIChomozygous126526827
76349232263492323GA12GENIChomozygous126616408
76349601563496016CT18GENIChomozygous126526829
76349616263496163CT24GENIChomozygous126526831
76349629763496298AC19GENIChomozygous126526833
76349844863498449GA5GENICheterozygous126526835
76350094263500943AG15GENIChomozygous126526837