chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4224572733224572734CT24GENIChomozygous57111274
4224573209224573210TC17GENIChomozygous57111276
4224573259224573261TG--13GENIChomozygous57111278
4224573304224573305TG10GENIChomozygous57111280
4224573813224573814T-11GENICheterozygous57111282
4224573816224573817TTCC17GENICpossibly homozygous57111284
4224573817224573818TTC19GENICpossibly homozygous57111286
4224574455224574456TC27GENIChomozygous57111288
4224575209224575210TC11GENIChomozygous57111290
4224575442224575443T-15GENIChomozygous57111292
4224575578224575579AG11GENICpossibly homozygous57111295
4224575699224575700GGA5GENIChomozygous57111297
4224575703224575704CCTTATGAGTGT2GENIChomozygous57111299
4224576326224576327AC25GENIChomozygous57111301
4224576402224576403GA23GENIChomozygous57111303
4224576561224576562TG24GENIChomozygous57111305
4224576594224576595AT24GENIChomozygous57111307
4224576851224576852AG25GENIChomozygous57111309
4224577057224577058CCA11GENIChomozygous57111311
4224577254224577255AG16GENIChomozygous57111312
4224577762224577766ACAG----19GENIChomozygous57111314
4224578284224578285A-16GENIChomozygous57111316
4224578306224578307AAAG19GENIChomozygous57111320
4224578387224578388AG32GENIChomozygous57111322
4224579979224579980TTG5GENIChomozygous57111324
4224580805224580806GC19GENIChomozygous57111328