chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2257007926257007927CT28GENIChomozygous110409991
2257009520257009521TC30GENIChomozygous110410001
2257010417257010418AG20GENIChomozygous110410007
2257018746257018747AG16GENIChomozygous110410031
2257019067257019068AG21GENIChomozygous110410033
2257019220257019221TC35GENIChomozygous110410037
2257019543257019544GT25GENIChomozygous120255816
2257019652257019653GA33GENIChomozygous110410041
2257019724257019725AC19GENIChomozygous120177457
2257019725257019726GC20GENIChomozygous120177458
2257020226257020227TC26GENIChomozygous110410043
2257022810257022811TC25GENIChomozygous110410049
2257023543257023544TC16GENIChomozygous110410055
2257023746257023747AG31GENIChomozygous111196278
2257023859257023860CT22GENIChomozygous111196280
2257024135257024136TC31GENIChomozygous111196282
2257024637257024638CT27GENIChomozygous111196284
2257026248257026249AG23GENIChomozygous110410069
2257027918257027919CT25GENIChomozygous110410077
2257028176257028177CT18GENIChomozygous111196292
2257028554257028555AG21GENIChomozygous110410079
2257029280257029281TG23GENIChomozygous111196294
2257029926257029927CT26GENIChomozygous110410081
2257032746257032747CT29GENIChomozygous110410083
2257033966257033967AC15GENIChomozygous110410085
2257034219257034220GA18GENIChomozygous110410087
2257035147257035148AG22GENIChomozygous110410089
2257036062257036063TC26GENIChomozygous110410091
2257036177257036178AG33GENIChomozygous110410093
2257036410257036411GA27GENIChomozygous110410095
2257038063257038064AG10GENIChomozygous110410097