chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135124175051241753GAC13GENIChomozygous131126472
135124278751242788GA9GENIChomozygous123733720
135124380951243809TCCTCCTCCTCCTTGTCCTCCTCC12GENIChomozygous131126473
135124277251242773AG9GENIChomozygous118598284
135124279051242791GA9GENIChomozygous118535434
135124277851242779AG9GENIChomozygous118498482
135124444951244450GC20GENIChomozygous114342955
135124376351243764CT18GENIChomozygous114890565
135124516751245168TC6GENIChomozygous114857637
135124619251246194GA9GENIChomozygous131126474
135124628751246288GA20GENIChomozygous114342971
135124632951246330GA23GENIChomozygous114890567
135124771551247716T17GENICheterozygous133497066
135125006151250062AG15GENIChomozygous114890569
135125241551252416TA27GENIChomozygous114343009
135125283451252835GA20GENIChomozygous114343011
135125430251254303AG29GENIChomozygous114343017
135125657751256597TTGGCTCAGTGGTAGAGCGC14GENIChomozygous129053099
135125699151256992TC34GENIChomozygous114890571
135125712851257129TC27GENICpossibly homozygous114890573
135125714351257144AG29GENICpossibly homozygous114890575
135125767151257672GC24GENIChomozygous114890577
135125782151257822T19GENICheterozygous129053100
135125803551258036T18GENIChomozygous129053101
135125806751258068CT17GENIChomozygous114890579
135125825151258252GA28GENIChomozygous114890581
135125827151258275GAAA27GENIChomozygous131126475
135125833851258339AC22GENIChomozygous115010053
135125887351258874GA19GENIChomozygous114890583
135125891751258918GA18GENIChomozygous114890585
135125891851258919GA17GENIChomozygous114890587
135125925751259258CT18GENIChomozygous114890589
135125132551251326GA20GENIChomozygous114672315