chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4140887210140887211TG26GENIChomozygous807236327
4140887405140887406GC61GENIChomozygous807236328
4140887526140887527AG58GENIChomozygous807236329
4140889290140889291CA65GENICheterozygous807236330
4140892114140892115TA37GENIChomozygous807236331
4140892182140892183AT37GENICheterozygous807236332
4140894149140894150GA52GENIChomozygous807236333
4140894483140894484TC40GENIChomozygous807236334
4140894658140894659GC72GENIChomozygous807236335
4140895871140895872GA45GENICheterozygous807236336
4140896988140896989GA50GENIChomozygous807236337
4140899328140899329GA64GENIChomozygous807236338
4140901019140901020TC39GENICpossibly homozygous807236339
4140902715140902716TC42GENIChomozygous807236340
4140902957140902958AG36GENIChomozygous807236341
4140903807140903808CT42GENIChomozygous807236342
4140904293140904294CG13GENIChomozygous807236343
4140904305140904306TC6GENIChomozygous807236344
4140906395140906396AG60GENICpossibly homozygous807236345
4140907673140907674TC49GENICheterozygous807236346
4140908274140908275TG52GENIChomozygous807236347
4140908994140908995GC46GENIChomozygous807236348
4140909042140909043GA58GENIChomozygous807236349
4140909059140909060CA55GENICpossibly homozygous807236350
4140909109140909110GA46GENIChomozygous807236351
4140909129140909130CT47GENICpossibly homozygous807236352
4140909170140909171GA50GENIChomozygous807236353
4140909196140909197CT50GENIChomozygous807236354
4140909244140909245GT52GENIChomozygous807236355
4140909248140909249TA54GENIChomozygous807236356
4140909269140909270GA48GENIChomozygous807236357
4140909286140909287GC48GENICpossibly homozygous807236358
4140913023140913024AG43GENIChomozygous807236359
4140913522140913523CT20GENICpossibly homozygous807236360
4140916630140916631TG54GENIChomozygous807236361
4140916631140916632CA53GENIChomozygous807236362
4140916937140916938GA53GENICpossibly homozygous807236363