chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2206224804206224805TC22GENIChomozygous110215528
2206224899206224900TC29GENIChomozygous110215529
2206228269206228270AG32GENIChomozygous110215532
2206229129206229130CA26GENIChomozygous110215533
2206230616206230617TC19GENIChomozygous110215534
2206232685206232686CG21GENIChomozygous110215535
2206233088206233089GA27GENIChomozygous110215536
2206233102206233103CG30GENIChomozygous110215537
2206237599206237600AG27GENIChomozygous110215538
2206238714206238715CT12GENIChomozygous110215539
2206240186206240187CT19GENIChomozygous110215540
2206242469206242470AT26GENIChomozygous110215541
2206242639206242640AG15GENIChomozygous110215542
2206243093206243094AG20GENIChomozygous110215543
2206244490206244491CT18GENIChomozygous110215544
2206246333206246334AG10GENIChomozygous110215545
2206246905206246906GA28GENIChomozygous110215546
2206249931206249932CT15GENIChomozygous110215547
2206251172206251173CT16GENICpossibly homozygous110215548
2206251820206251821AT9GENIChomozygous110215549
2206252336206252337TA14GENIChomozygous110215550
2206253817206253818AC15GENIChomozygous110215551
2206255229206255230AC19GENIChomozygous110215553
2206256098206256099GA21GENIChomozygous110215554
2206257072206257073GA24GENIChomozygous110215555
2206258753206258754CA24GENIChomozygous110215556
2206260580206260581GA18GENIChomozygous110215557
2206262977206262978CA24GENIChomozygous110215558
2206265162206265163TA27GENIChomozygous110215559
2206265806206265807GA14GENIChomozygous110215560
2206270974206270975GA11GENIChomozygous110215561
2206271785206271786TC19GENIChomozygous110215563
2206271895206271896TC21GENIChomozygous110215564
2206273037206273038TC16GENIChomozygous110215566
2206274739206274740CG16GENIChomozygous110215567
2206274840206274841TC20GENIChomozygous110215568