chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101158837811588379TC23GENIChomozygous138725258
101158846411588465GC21GENIChomozygous145733090
101158969011589691TC24GENIChomozygous143441097
101158981411589815AG19GENIChomozygous138725260
101159123011591231GA23GENIChomozygous145733091
101159126511591266AG23GENIChomozygous138725261
101159167111591672CT31GENIChomozygous145733092
101159246411592465AT17GENICpossibly homozygous145733093
101159511611595117GA29GENIChomozygous145733094
101159617111596172TG20GENIChomozygous145733095
101159708511597086GA21GENIChomozygous145733096
101159819011598191AT19GENIChomozygous138725267
101159861811598619GA20GENIChomozygous145733097
101159544611595448GT21GENIChomozygous138668869
101159569311595693AGAC24GENIChomozygous138668870
101160173811601739T10GENIChomozygous138668872
101160360711603608TC18GENIChomozygous138725276
101160372511603726AT21GENIChomozygous138725277
101160476311604764AG19GENIChomozygous138725280
101160504111605042AG27GENIChomozygous138725281
101160533011605336ACAGAC16GENIChomozygous145727386
101160615211606153GA21GENIChomozygous145733098
101160656711606567T12GENICpossibly homozygous145727387
101160851311608514GT26GENIChomozygous145733099
101160864711608648TC23GENIChomozygous145733100
101160924111609242CT31GENIChomozygous145733101
101161015911610160TG24GENIChomozygous145733102
101161219811612199CT21GENIChomozygous143441108
101161240311612404TC22GENIChomozygous138725284
101161240911612410AG23GENIChomozygous138725285
101161396911613970AC24GENIChomozygous138725287
101161614511616146AG25GENIChomozygous145733103
101161683511616836C18GENIChomozygous145727388
101161693911616940TC20GENIChomozygous145733104
101161793911617939AAG20GENIChomozygous145727389
101161855811618559CT21GENIChomozygous142213594