chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2207437429207437430CT20GENIChomozygous110907534
2207437752207437754GA16GENIChomozygous132019205
2207439071207439072GA22GENIChomozygous110907535
2207439263207439264AG25GENIChomozygous110907536
2207440448207440449TC31GENIChomozygous111282840
2207441103207441104AC12GENIChomozygous110907537
2207441114207441114A15GENIChomozygous132019206
2207441152207441153CT23GENIChomozygous110907538
2207441821207441822TC22GENIChomozygous110907539
2207442076207442077CT23GENIChomozygous110907540
2207442340207442341GC18GENIChomozygous111282842
2207443057207443059TA14GENIChomozygous132019207
2207443335207443336GA19GENIChomozygous111282844
2207443691207443692TC22GENIChomozygous110907542
2207444147207444148AG20GENIChomozygous110907544
2207444543207444544T29GENIChomozygous132019208
2207444646207444647GA25GENIChomozygous111282846
2207444844207444852TGCGTGCA21GENICheterozygous132019209
2207445885207445886GA27GENIChomozygous111282848
2207446139207446140A23GENIChomozygous132019210
2207446190207446191CT20GENIChomozygous111282850
2207446191207446192AG20GENIChomozygous111282852
2207446241207446242TG14GENIChomozygous111282854
2207446751207446752TC19GENIChomozygous110907546
2207447014207447015CT25GENIChomozygous111282856
2207447560207447560GG21GENIChomozygous132019212
2207449399207449400CT18GENIChomozygous111282858
2207449591207449592TC18GENIChomozygous110907549
2207449843207449844AG18GENIChomozygous111282860
2207449858207449859CT19GENIChomozygous111282862
2207450762207450763T15GENIChomozygous132019214
2207451316207451317G18GENIChomozygous132019215
2207453364207453365CT19GENIChomozygous111282864
2207456551207456552AC14GENIChomozygous110907552
2207441727207441728AG16GENIChomozygous110217055
2207447560207447561CT19GENIChomozygous120173066