chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1205960583205960584T-17GENICheterozygous62248620
1205964534205964535GA31GENIChomozygous62695013
1205965265205965266TTA9GENICheterozygous62192717
1205965266205965267A-9GENICheterozygous61065929
1205967347205967348CCT4GENIChomozygous62192719
1205967704205967705AAT7GENICheterozygous62192721
1205967705205967707TT--7GENICheterozygous61065934
1205967706205967707T-7GENICheterozygous61065935
1205968130205968131T-24GENICpossibly homozygous61065937
1205968132205968133TG23GENICpossibly homozygous62695014
1205969527205969529TT--14GENICheterozygous61065942
1205969528205969529T-14GENICheterozygous62192723
1205979235205979236T-13GENICheterozygous62192725
1205980359205980361TT--14GENICheterozygous61318353
1205980360205980361T-14GENICheterozygous62248622
1205982040205982042TA--22GENICheterozygous61065949
1205984611205984612GA22GENIChomozygous62695015
1206000226206000228GG--5GENICheterozygous62192727
1206004902206004903TG23GENIChomozygous61065956
1206004990206004991T-7GENICheterozygous61065957
1206005016206005018TT--7GENICheterozygous62030738
1206015381206015382CCT6GENICheterozygous62561602