chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2207437429207437430CT28GENIChomozygous110907534
2207437752207437754GA28GENIChomozygous132019205
2207439071207439072GA33GENIChomozygous110907535
2207439263207439264AG30GENIChomozygous110907536
2207440448207440449TC22GENIChomozygous111282840
2207441103207441104AC18GENIChomozygous110907537
2207441114207441114A18GENIChomozygous132019206
2207441152207441153CT20GENIChomozygous110907538
2207441821207441822TC27GENIChomozygous110907539
2207442076207442077CT19GENIChomozygous110907540
2207442340207442341GC18GENIChomozygous111282842
2207442840207442841T17GENICheterozygous132387080
2207443057207443059TA26GENIChomozygous132019207
2207443335207443336GA20GENIChomozygous111282844
2207443691207443692TC23GENIChomozygous110907542
2207444147207444148AG31GENIChomozygous110907544
2207444543207444544T22GENIChomozygous132019208
2207444646207444647GA30GENIChomozygous111282846
2207444844207444852TGCGTGCA20GENICpossibly homozygous132019209
2207445885207445886GA23GENIChomozygous111282848
2207446139207446140A29GENIChomozygous132019210
2207446190207446191CT23GENIChomozygous111282850
2207446191207446192AG23GENIChomozygous111282852
2207446241207446242TG24GENIChomozygous111282854
2207446751207446752TC22GENIChomozygous110907546
2207447014207447015CT23GENIChomozygous111282856
2207447560207447561CT33GENIChomozygous120173066
2207447560207447560GG34GENIChomozygous132019212
2207449399207449400CT27GENIChomozygous111282858
2207449591207449592TC28GENIChomozygous110907549
2207449843207449844AG26GENIChomozygous111282860
2207449858207449859CT28GENIChomozygous111282862
2207450762207450763T30GENIChomozygous132019214
2207451316207451317G23GENIChomozygous132019215
2207453364207453365CT23GENIChomozygous111282864
2207456551207456552AC22GENIChomozygous110907552
2207441727207441728AG23GENIChomozygous110217055