chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1038795693879570TC22GENIChomozygous116471646
1039068493906850GC4GENIChomozygous117977147
1039178253917826CA53GENICheterozygous117977149
1039178943917895CA54GENICheterozygous117977153
1039409363940937CT68GENICheterozygous118073564
1039409413940942CA55GENICheterozygous117977175
1039410763941077CA36GENICheterozygous118073565
1039411233941124AG40GENICheterozygous118073566
1039415353941536CA72GENICheterozygous117977179
1039423663942367CT45GENICheterozygous118073567
1039424203942421CT15GENICpossibly homozygous117977191
1039424593942460CT31GENICpossibly homozygous118060083
1039426733942674GA48GENICheterozygous117977208
1039750663975067AG19GENIChomozygous116471892
1039750823975083TC19GENIChomozygous116910624
1039867933986794GT21GENICheterozygous118073568
1040154954015496CT26GENICpossibly homozygous118060088
1040155214015522TC29GENICheterozygous118060090
1040272004027201GA39GENICheterozygous118023338
1040885034088504TC58GENICheterozygous118023428
1040886424088643GA40GENICheterozygous118073569
1040888414088842AG60GENICheterozygous117977387
1040892094089210AG172GENICheterozygous117977413
1040896364089637AC219GENICheterozygous117977422
1040896384089639AG216GENICheterozygous118060096
1040896874089688CA206GENICheterozygous118023442
1040900324090033AG94GENICheterozygous118060098
1040901514090152GA52GENICheterozygous117977443
1041484104148411GT13GENICheterozygous116472272
1041484114148412GC14GENICpossibly homozygous116472274
1041498114149812AG39GENIChomozygous116472276
1041593024159303AC41GENICheterozygous118073570
1041603334160334GT42GENIChomozygous116472290
1041986354198636TC11GENIChomozygous117073986
1042222224222223TG13GENIChomozygous116472443
1042300444230045TC23GENIChomozygous116472457
1042468784246879CA11GENICpossibly homozygous116472509