chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1221487124221487125TC25GENICpossibly homozygous108994917
1221487492221487493AC18GENIChomozygous108994918
1221488111221488112AC9GENIChomozygous108994919
1221488939221488940TC23GENIChomozygous108994920
1221488991221488992CT21GENIChomozygous108994921
1221489445221489446GA12GENIChomozygous108994922
1221489591221489592CT19GENICheterozygous120512306
1221489752221489753CT17GENIChomozygous108994923
1221490050221490051GT16GENIChomozygous108994924
1221490330221490331CG21GENIChomozygous108994925
1221490334221490335GA22GENIChomozygous108994926
1221490351221490352GA23GENIChomozygous108994927
1221490560221490561CT23GENIChomozygous108994928
1221491334221491335TC13GENIChomozygous108994929
1221492059221492060TC25GENIChomozygous108994930
1221492358221492359CG23GENIChomozygous108994931
1221492479221492480TC28GENIChomozygous108994932
1221492581221492582AT16GENICpossibly homozygous108994933
1221492899221492900CA29GENICpossibly homozygous108994934
1221493294221493295GA33GENIChomozygous108994935
1221493361221493362TC24GENIChomozygous108994936
1221493432221493433AG22GENIChomozygous108994937
1221494395221494396TC16GENIChomozygous108994940
1221494872221494873TA16GENIChomozygous108994943