chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
12408950524089506AG31GENIChomozygous601148458
12408956824089569TC38GENIChomozygous601148459
12409026924090270AAC11GENICpossibly homozygous729514297
12409035624090357GA28GENIChomozygous603374295
12409049724090498CT34GENIChomozygous603374296
12409303324093034AT41GENIChomozygous603374297
12409310424093105C-32GENIChomozygous729514298
12409320524093206GA37GENIChomozygous601148460
12409346724093468CT30GENIChomozygous603374298
12409454724094548CCAAA24GENIChomozygous729514299
12409455124094552CA24GENIChomozygous603374299
12409455224094553TG24GENIChomozygous603374300
12409486724094868TTTTTA36GENIChomozygous729514300
12409578724095788CT27GENIChomozygous603374301
12409697924096980AG32GENIChomozygous601148461
12409728724097288AC23GENIChomozygous601148462
12409800824098009AC22GENIChomozygous601148463
12409805524098056CT27GENIChomozygous603374302
12409830724098308TC30GENIChomozygous603374303
12409864224098643GC40GENIChomozygous601148464
12409896324098964CG22GENIChomozygous601148465
12409896424098965AG22GENIChomozygous603374304
12409897424098975AT26GENIChomozygous603374305
12409897524098976AG26GENIChomozygous603374306
12409898024098983GAC---30GENIChomozygous729514301
12409898424098985AATTT26GENIChomozygous729514302
12409898524098986GT27GENIChomozygous603374307
12409931624099317GA19GENIChomozygous603374308
12409932824099329AC21GENIChomozygous601148466
12409959024099591TTA22GENICheterozygous729514303
12409959024099591TTAAAAAAAAAAA22GENICheterozygous729514304