chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3142220321142220322GC25GENIChomozygous143030284
3142226057142226058GC10GENICheterozygous403080851
3142226057142226058G10GENICpossibly homozygous403080852
3142226059142226060GC10GENICheterozygous403080853
3142226059142226060G10GENICpossibly homozygous403080854
3142226061142226062GC10GENICheterozygous403080855
3142226061142226062G10GENICpossibly homozygous403080856
3142228020142228021C10GENICheterozygous403080859
3142228020142228021CT10GENIChomozygous403080860
3142231185142231186TA17GENIChomozygous143030285
3142231882142231883AG29GENIChomozygous143030286
3142233173142233174TG25GENIChomozygous143030287
3142233815142233816GA25GENIChomozygous143030288
3142234042142234043AG19GENIChomozygous143030289
3142235446142235447GA21GENIChomozygous143030290
3142236850142236851CT15GENIChomozygous143030291
3142237171142237172CT23GENIChomozygous143030292
3142237205142237206TC25GENIChomozygous143030293
3142238764142238765AG12GENIChomozygous143030294
3142241661142241662TC31GENIChomozygous143030295
3142242660142242661TC19GENIChomozygous143030296
3142242751142242752CT28GENIChomozygous143030297
3142242911142242912GA10GENIChomozygous143030298
3142243709142243710CT24GENIChomozygous143030299
3142244004142244005GA16GENIChomozygous143030300
3142244745142244746AG23GENIChomozygous143030301
3142244746142244747AG23GENIChomozygous143030302
3142244830142244831CT19GENIChomozygous143030303
3142245676142245677TC25GENIChomozygous143030304
3142246598142246599TG19GENIChomozygous143030305
3142239229142239232ATT13GENICheterozygous143865258
3142229725142229729CTCC6GENIChomozygous143002954
3142231735142231735T16GENIChomozygous143002955
3142232272142232272A26GENIChomozygous143002956