chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
37259037072590371CG48GENICheterozygous112127654
37259039572590396CG84GENICpossibly homozygous112127655
37259049672590497GC59GENICheterozygous112232791
37259057272590573TC32GENIChomozygous112127656
37259066672590667CG32GENIChomozygous112127657
37259070672590707CT34GENIChomozygous111608283
37259080672590807AG41GENIChomozygous111608284
37259089072590891AG30GENIChomozygous112127658
37259179172591792AG26GENIChomozygous111608286
37259252772592528AG20GENIChomozygous111608288
37259256172592562TC20GENIChomozygous111608289
37259288172592882CT18GENIChomozygous112127659
37259331472593315AC12GENIChomozygous112127660
37259343872593439GA25GENIChomozygous112127661
37259361672593617CA17GENIChomozygous112127662
37259392772593928GA22GENIChomozygous111608293
37259457672594577TC29GENIChomozygous111608295
37259489372594894CA30GENIChomozygous111608297
37259596772595968CT28GENIChomozygous112127663
37259622372596224TC32GENIChomozygous111608305
37259774472597745GA35GENIChomozygous112127664
37259862872598629TC15GENIChomozygous112127665
37259886172598862TC17GENIChomozygous111608308
37260171472601715AG24GENICheterozygous112343080
37260172372601724AG22GENICheterozygous112127666
37260184072601841TC39GENIChomozygous111608310
37260227572602276CT40GENICpossibly homozygous112127667
37260257872602579GA30GENIChomozygous112127668
37260299372602994TG48GENIChomozygous111608312
37260315572603156CT36GENIChomozygous112127669
37260409272604093AG29GENIChomozygous111608313
37260420872604209AT28GENIChomozygous111608314
37260459072604591CT30GENIChomozygous111608315