chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
79183380191833801A19GENICheterozygous131021030
79183408891834088A34GENIChomozygous128493411
79183477491834774ATTCCTGTTAAAATAG43GENIChomozygous128493412
79183608591836085TC26GENIChomozygous131681303
79183612891836129TC15GENIChomozygous116051315
79183670091836702AT7GENIChomozygous131873195
79183783691837836A36GENIChomozygous131873196
79184197791841979TA28GENICpossibly homozygous128493413
79184401891844019TC9GENICheterozygous131881020
79184525391845254GT50GENIChomozygous116051317
79184568891845689T47GENICpossibly homozygous128493414
79184786791847867A46GENIChomozygous128493415
79185679391856794CT49GENIChomozygous116051319
79185896891858969GA22GENIChomozygous116051321
79186856191868562GA46GENIChomozygous116051325
79186256091862561GT25GENICheterozygous132119017
79185356491853565CT51GENIChomozygous115761191
79185702991857030TC51GENIChomozygous115761195
79184540591845419GCACACATGCACAC47GENIChomozygous132111190
79186253591862536C16GENICheterozygous132111191
79186255791862558CT24GENICheterozygous132119016