chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5150689860150689861A-2GENICheterozygous55794303
5150691202150691203AG18GENICpossibly homozygous55794307
5150691959150691960TC11GENIChomozygous55794308
5150692638150692639TC16GENIChomozygous55794311
5150693001150693002AG2GENIChomozygous55794312
5150693275150693276AG10GENIChomozygous55794313
5150693616150693617TC20GENICpossibly homozygous55794314
5150693673150693674AG18GENICpossibly homozygous55794315
5150693730150693731TC13GENIChomozygous55794316
5150695158150695159AG11GENIChomozygous55794318
5150695273150695274TC10GENIChomozygous55794319
5150695708150695709CT13GENICpossibly homozygous55794321
5150696202150696203TC14GENIChomozygous55794322
5150696582150696583GC11GENIChomozygous55794323
5150696871150696872AATG3GENICheterozygous56936742
5150696929150696930AATG1GENIChomozygous55794332
5150698648150698649CT17GENICpossibly homozygous55794334
5150700645150700646GA6GENIChomozygous55794335
5150702261150702262GT10GENICheterozygous55794336
5150703291150703292GT11GENICpossibly homozygous55794337
5150703488150703489GT15GENICpossibly homozygous55794338
5150712090150712091CCCAGGCTCTGCCG4GENIChomozygous55794342
5150713327150713328GGTGAATGAT4GENIChomozygous55794343
5150714195150714196CCAAA2GENICheterozygous56128680