chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1268771038268771039GA13GENIChomozygous108640919
1268771279268771280GT16GENIChomozygous108640920
1268771874268771875TC26GENIChomozygous108640925
1268772121268772122CA9GENIChomozygous108640926
1268772341268772342TC4GENIChomozygous108640928
1268772587268772588GA23GENIChomozygous108640930
1268772644268772645CT11GENIChomozygous108640931
1268772714268772715TA17GENIChomozygous108640932
1268772865268772866TC4GENIChomozygous108640935
1268773032268773033CG12GENIChomozygous108640936
1268773066268773067GA17GENIChomozygous108640937
1268773168268773169CT13GENIChomozygous108640938
1268773397268773398CA17GENIChomozygous108640939
1268773488268773489AG6GENIChomozygous108640940
1268773898268773899GT10GENIChomozygous125328402
1268774041268774042GT17GENIChomozygous108640941
1268774101268774102AG20GENIChomozygous108640942
1268774357268774358CG20GENIChomozygous108640943
1268774569268774570AG18GENIChomozygous108640944
1268775615268775616TG10GENIChomozygous108640945
1268775805268775806CT15GENIChomozygous108640946
1268776100268776101CA5GENIChomozygous108640953
1268776226268776227AG15GENIChomozygous108640955
1268776306268776307CT26GENIChomozygous108640956
1268776360268776361CT17GENIChomozygous108640957
1268776398268776399AT15GENIChomozygous108640958
1268776557268776558CT9GENIChomozygous108640959
1268776910268776911AC15GENIChomozygous108640960
1268777153268777154TC8GENIChomozygous109379827
1268777359268777360TA4GENIChomozygous108640962
1268780423268780424CA6GENIChomozygous120846776
1268781920268781921CT21GENIChomozygous108640995
1268781975268781976AG15GENIChomozygous108786297
1268778206268778207TC19GENIChomozygous108786293
1268781746268781747GA8GENIChomozygous108786295
1268781801268781802CT19GENIChomozygous108786296
1268782047268782048GA12GENIChomozygous108640996
1268782099268782100CT16GENIChomozygous108786298