chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10102869000102869002GT--25GENICheterozygous52605232
10102869887102869888AT15GENIChomozygous52327350
10102869931102869932TG15GENIChomozygous51587804
10102869936102869937TG16GENIChomozygous51587806
10102869940102869941AC15GENIChomozygous51587808
10102869946102869947GC16GENIChomozygous51587810
10102869949102869950TC17GENIChomozygous51587812
10102869967102869968TA18GENIChomozygous51587814
10102869970102869971AT18GENIChomozygous51587816
10102869977102869978GC19GENIChomozygous51587818
10102876440102876444GAAG----4GENICheterozygous52913233
10102876510102876511AAG3GENIChomozygous51587822
10102876517102876518AAG2GENIChomozygous51587824
10102879975102879977GT--2GENICheterozygous52403996
10102885891102885892A-16GENICheterozygous52651683
10102891820102891821AG10GENIChomozygous51587826
10102891926102891927GT29GENIChomozygous51587828
10102891941102891942AC21GENIChomozygous52327354
10102891943102891944CA24GENIChomozygous52327357
10102891950102891951GC20GENIChomozygous51587830
10102891953102891954TG21GENIChomozygous51587832
10102891964102891965AG22GENIChomozygous51587834
10102891969102891970A-23GENIChomozygous51587836
10102891973102891974GC24GENIChomozygous51587838
10102891976102891977AG22GENIChomozygous51587840
10102891979102891980AG22GENIChomozygous51587842
10102891983102891984GGC23GENIChomozygous51587844
10102891984102891985GA23GENIChomozygous52327359
10102891989102891990TA21GENIChomozygous52327361
10102897490102897491TTACAC10GENICheterozygous52403998
10102897491102897493AC--10GENICheterozygous52404000
10102898736102898737A-13GENICheterozygous51998927
10102900567102900569AC--6GENICheterozygous52404002