chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
51852061118520612TC16GENIChomozygous55225894
51852061918520620A-17GENIChomozygous55225895
51852065218520653AG22GENIChomozygous55225896
51852128118521282GT11GENIChomozygous55225897
51852144018521441GT8GENIChomozygous55225898
51852151518521516TA13GENIChomozygous55225899
51852163118521632AG16GENIChomozygous55225900
51852167718521678CG23GENIChomozygous55225901
51852211118522112CT20GENIChomozygous55225902
51852221618522217CT22GENIChomozygous55225903
51852224618522247GA21GENIChomozygous55225904
51852237918522380CG25GENIChomozygous55225905
51852272018522721CT10GENIChomozygous55225906
51852290718522908TC17GENIChomozygous55225907
51852346518523466AG15GENIChomozygous55225908
51852356518523566CT22GENIChomozygous55225909
51852428018524281CA12GENIChomozygous55225910
51852438518524386CA16GENIChomozygous55225911
51852451518524516CT14GENIChomozygous55225912
51852475418524755TC14GENIChomozygous55225913
51852511118525112AC17GENIChomozygous55225914
51852513118525132TA23GENIChomozygous55225916
51852587618525877CT14GENIChomozygous55225917
51852609118526092CT22GENIChomozygous55225918
51852619918526200TC22GENIChomozygous55225919
51852625818526259TA26GENIChomozygous55225920
51852659418526595AG13GENIChomozygous55225921
51852686018526861AAAG12GENIChomozygous55225922
51852786718527868TC13GENIChomozygous55225923
51852803018528031GA15GENIChomozygous55225924
51852920118529202AG20GENIChomozygous55225925
51852986218529863TC22GENIChomozygous55225928
51853014118530142GC17GENICpossibly homozygous55225931
51853048118530482AG29GENIChomozygous55225932
51853060318530604GA25GENIChomozygous55225933
51853098018530981TA22GENIChomozygous55225934
51853269418532695CT27GENIChomozygous55225935
51853294918532950GGCACACACACACA6GENICheterozygous56485752
51853337818533386ACACACAC--------8GENIChomozygous55864880
51852966818529669TTG18GENIChomozygous55977578
51853011918530120GGAA6GENICheterozygous56397561
51853294918532950GGCACACACACA6GENICheterozygous56397564