chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101967353619673537AT17GENIChomozygous141037718
101967354519673546CT15GENIChomozygous141037719
101967354919673550CG15GENIChomozygous403773928
101967354919673550CT15GENICheterozygous403773929
101973977919739779AG3GENICheterozygous141036955
101974303519743036G15GENICheterozygous403278436
101974303519743036GC15GENIChomozygous403278437
101980939019809391GC10GENICpossibly homozygous138732485
101980939919809400AG11GENICheterozygous403278472
101980939919809400A11GENICheterozygous403278473
101980940519809406AG10GENICheterozygous403278476
101980940519809406A10GENICheterozygous403278477
101985653919856540TA17GENICheterozygous141037720
101988589019885891GT2GENIChomozygous138732565
101997082619970827GC6GENICheterozygous403278516
101997082619970827G6GENICheterozygous403278517
101997082819970829GC6GENICheterozygous403278518
101997082819970829G6GENICheterozygous403278519
101997945519979456AG10GENICheterozygous154623066
101997945519979456A10GENICheterozygous403278531
102002414820024149T7GENICheterozygous403278541
102002414820024149TA7GENICheterozygous403278542
102003613020036131T21GENICheterozygous141094775
102006979820069799AG20GENICheterozygous154629610
102006979820069799A20GENICheterozygous403632155
102006979920069800AG20GENICheterozygous403632156
102006979920069800A20GENICheterozygous403632157
102014113320141134A14GENICheterozygous141036957