chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
9100421014100421015TTA8GENICheterozygous52076895
9100421015100421016A-8GENICheterozygous52446888
9100421536100421537GT32GENIChomozygous52446890
9100422127100422128CT33GENIChomozygous52076897
9100423062100423063AG33GENIChomozygous52076899
9100424225100424226A-11GENICheterozygous52076903
9100427518100427519TA31GENIChomozygous52446892
9100427755100427756TC24GENIChomozygous52446894
9100428241100428242CT25GENIChomozygous52446896
9100428446100428447AAGT10GENICheterozygous52076907
9100429133100429134CT23GENIChomozygous52446898
9100429739100429740GGA17GENICpossibly homozygous52446900
9100430572100430574AA--9GENICheterozygous52076913
9100430573100430574A-9GENICheterozygous52076915
9100430678100430679C-16GENIChomozygous52446902
9100430757100430758GT26GENIChomozygous52076917
9100430924100430925TA18GENIChomozygous52446904
9100431327100431328TC23GENIChomozygous52446906
9100432151100432152TC21GENIChomozygous52446908
9100432401100432402G-15GENIChomozygous52446910
9100432453100432455TT--13GENICpossibly homozygous52446912
9100432454100432455T-13GENICheterozygous52076921
9100432887100432888GA18GENIChomozygous52076923
9100433023100433024TTC31GENIChomozygous52076927
9100433290100433291AC43GENICheterozygous52076929
9100433293100433294CCGAA41GENICheterozygous52076931