chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1226976799226976800CT20GENIChomozygous109198369
1226976832226976833CT19GENIChomozygous108998577
1226977116226977117GC13GENICheterozygous120512342
1226977118226977119GC13GENICheterozygous120512343
1226977120226977121GC11GENICheterozygous120512344
1226977122226977123GC9GENICheterozygous120512345
1226977124226977125GC10GENICheterozygous120512346
1226977126226977127GC10GENICheterozygous120512347
1226977128226977129GC10GENICheterozygous120512348
1226978653226978654CG16GENICheterozygous120512349
1226978654226978655TG17GENICheterozygous120512350
1226978655226978656AG17GENICheterozygous120512351
1226982312226982313GA20GENIChomozygous109198373
1226984444226984445GA6GENIChomozygous109198375
1226986081226986082GC27GENIChomozygous108998589
1226986192226986193AC18GENIChomozygous109198383
1226986533226986534AG20GENIChomozygous108998592
1226987423226987424AG15GENIChomozygous108998593
1226987756226987757TC14GENIChomozygous108998594
1226990074226990075TC24GENIChomozygous109198385
1226990176226990177GA24GENIChomozygous109198387
1226990504226990505CT27GENIChomozygous108998597
1226992745226992746TA35GENIChomozygous108998600
1226993297226993298CT29GENIChomozygous109198391