chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2207437429207437430CT11GENIChomozygous110907534
2207439071207439072GA26GENIChomozygous110907535
2207439263207439264AG21GENIChomozygous110907536
2207440448207440449TC18GENIChomozygous111282840
2207441103207441104AC25GENIChomozygous110907537
2207441152207441153CT20GENIChomozygous110907538
2207441727207441728AG15GENIChomozygous110217055
2207441821207441822TC10GENIChomozygous110907539
2207442076207442077CT17GENIChomozygous110907540
2207442340207442341GC16GENIChomozygous111282842
2207442838207442839TG15GENIChomozygous110907541
2207443335207443336GA14GENIChomozygous111282844
2207443691207443692TC14GENIChomozygous110907542
2207444147207444148AG20GENIChomozygous110907544
2207444646207444647GA7GENIChomozygous111282846
2207444851207444852AG11GENIChomozygous125701444
2207445885207445886GA28GENIChomozygous111282848
2207446190207446191CT24GENIChomozygous111282850
2207446191207446192AG24GENIChomozygous111282852
2207446241207446242TG23GENIChomozygous111282854
2207446751207446752TC16GENIChomozygous110907546
2207447014207447015CT21GENIChomozygous111282856
2207447552207447553TC9GENICheterozygous125726549
2207449399207449400CT10GENIChomozygous111282858
2207449591207449592TC18GENIChomozygous110907549
2207449843207449844AG21GENIChomozygous111282860
2207449858207449859CT19GENIChomozygous111282862
2207453364207453365CT19GENIChomozygous111282864
2207456551207456552AC13GENIChomozygous110907552