chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4224572733224572734CT9GENIChomozygous57111274
4224573209224573210TC21GENIChomozygous57111276
4224573259224573261TG--11GENIChomozygous57111278
4224573304224573305TG20GENIChomozygous57111280
4224573816224573817TTCC16GENICpossibly homozygous57111284
4224573816224573817TTC16GENICheterozygous58307074
4224574455224574456TC36GENIChomozygous57111288
4224575209224575210TC25GENIChomozygous57111290
4224575442224575443T-31GENIChomozygous57111292
4224575513224575525TCTCTCTCTCTC------------13GENIChomozygous58307076
4224575578224575579AG9GENIChomozygous57111295
4224575699224575700GGA27GENIChomozygous57111297
4224575702224575703AT28GENIChomozygous58307078
4224575703224575704CCTTATGAGTGT27GENIChomozygous57111299
4224575704224575705CT27GENIChomozygous58307080
4224576326224576327AC20GENIChomozygous57111301
4224576402224576403GA29GENIChomozygous57111303
4224576561224576562TG24GENICpossibly homozygous57111305
4224576594224576595AT23GENIChomozygous57111307
4224576851224576852AG15GENIChomozygous57111309
4224577057224577058CCA25GENICheterozygous57111311
4224577254224577255AG24GENIChomozygous57111312
4224577762224577766ACAG----24GENIChomozygous57111314
4224578284224578285A-10GENIChomozygous57111316
4224578306224578307AAAG22GENICpossibly homozygous57111320
4224578387224578388AG23GENIChomozygous57111322
4224579990224579991TG5GENIChomozygous57111326
4224580805224580806GC22GENICpossibly homozygous57111328