chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103648769236487693TTA12GENICheterozygous52139481
103648794836487949GT20GENIChomozygous51414343
103648818836488189CT18GENICheterozygous52139483
103648825936488260TC15GENIChomozygous51414345
103648877536488776CA14GENIChomozygous51414347
103648962336489624AG11GENICheterozygous51414349
103649072836490729AG18GENIChomozygous51414351
103649144136491442A-16GENIChomozygous51414353
103649151936491520GA18GENIChomozygous51414355
103649259336492594CA14GENICheterozygous53517699
103648936936489370CT16GENICheterozygous53517693
103648997436489975AT16GENICheterozygous53517695
103649135536491356AG19GENICheterozygous53517697
103649287736492878AG16GENICheterozygous51414359
103649350536493506AG19GENIChomozygous51414361
103649355936493560AG17GENIChomozygous51414363
103649385536493857TA--12GENICheterozygous53517701
103649473136494732TC17GENIChomozygous51414365
103649488036494881TC11GENIChomozygous51414367
103649524536495246T-12GENICheterozygous51414371
103649653836496539CT17GENICheterozygous53517703
103649678036496781AG24GENIChomozygous51414373
103649885336498854CG14GENICheterozygous53517705
103649927936499280T-14GENICheterozygous51414375
103649930836499309GGTT14GENICheterozygous53517707
103649941036499411GC16GENIChomozygous51414377
103650003136500032TTA29GENIChomozygous51414381
103650051136500512TA20GENIChomozygous51414383
103650169636501697AT17GENIChomozygous51414385
103650169736501698GC16GENIChomozygous51414387
103650186136501862GT16GENICheterozygous53517709
103650200836502009TC14GENICheterozygous51414389
103650215536502159GTAG----12GENIChomozygous51414391
103650326336503264GA13GENICheterozygous51414393
103650440936504410CG18GENIChomozygous51414395
103650505936505060CT17GENIChomozygous51414397
103650506736505068TG17GENIChomozygous51414399
103650508536505086TTA15GENICheterozygous51414401