chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
139056726490567265TTATC43GENICpossibly homozygous49960833
139058189790581898CCT25GENIChomozygous49858903
139058191090581911GGA29GENIChomozygous49858904
139058191490581915C-28GENIChomozygous49858905
139058361690583617C-5GENICheterozygous49858907
139060303290603033GGGTGCTTT20GENIChomozygous49858908
139061475090614751C-44GENIChomozygous49858909
139063299190632992TG44GENICheterozygous49960834
139065274490652745GGGA4GENIChomozygous49960835
139066215990662160AAC34GENIChomozygous49858912
139066668690666687AATT28GENIChomozygous49858913
139067076590670766GA17GENICheterozygous49858915
139067081490670818GGAG----6GENICheterozygous49858916
139067082390670825GG--6GENICheterozygous49858917
139067082790670838GAGGAGGAGGA-----------7GENICheterozygous49858918
139067083790670838A-6GENIChomozygous49858919
139067083790670838AAG5GENIChomozygous49858920
139067598890675990TC--8GENICpossibly homozygous49858921