chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104621729846217324ACAGGGCTCCTGGAAGGGCTAGGGCG36GENIChomozygous131092521
104621972446219729CAGGG37GENICpossibly homozygous131092522
104622005846220059TC64GENIChomozygous116585259
104622010546220106TC51GENIChomozygous116585261
104622200246222003TC25GENIChomozygous116585263
104622186946221869CA26GENIChomozygous128814179
104622021846220219CG53GENIChomozygous116877618
104622116646221167CG53GENIChomozygous116877620
104622250646222507TC37GENICpossibly homozygous116877622
104622254646222547GA47GENIChomozygous116877624
104622463546224636AG41GENIChomozygous116877628
104622477246224773AG44GENIChomozygous116877630
104622478846224789AC39GENIChomozygous116585267
104622502546225026AG41GENIChomozygous116877632
104622610746226108GA44GENIChomozygous116877634
104622611446226121GGCTCAG48GENIChomozygous131092523
104622618546226186CG42GENIChomozygous116877636
104622639346226394CT49GENIChomozygous116877638
104622703046227031AT38GENIChomozygous116877640
104622802746228028AG59GENIChomozygous116585273
104622803046228031GC59GENIChomozygous116877642
104622850346228504TC58GENIChomozygous116877644
104623021946230220GA50GENIChomozygous116877646
104623172246231723CA12GENIChomozygous116877648
104623217546232176TC30GENIChomozygous116877651
104623259346232594TA36GENIChomozygous116585283
104623356446233565TC50GENIChomozygous116877653
104624052846240529AT46GENIChomozygous116585291
104624185846241859TC50GENIChomozygous116585293
104623332746233328CT51GENIChomozygous118115378