chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3118618615118618616CT24GENIChomozygous57624280
3118618660118618661AG23GENIChomozygous57624282
3118618668118618669AC23GENIChomozygous57624284
3118619117118619124TTTTTTT-------3GENIChomozygous58620911
3118621248118621249CG17GENIChomozygous57624288
3118621367118621368CT20GENIChomozygous57624290
3118621810118621811AT17GENIChomozygous58015103
3118621834118621835GA16GENIChomozygous58015106
3118622991118622992GA17GENIChomozygous58015109
3118623023118623025TT--12GENICheterozygous58620912
3118623024118623025T-12GENICheterozygous58671469
3118623568118623569AG39GENIChomozygous57624298
3118624227118624228GGCACACA12GENIChomozygous59422082
3118626820118626821G-22GENIChomozygous57624308
3118627106118627114AAACAAAC--------21GENIChomozygous58620913
3118627804118627805CCT31GENIChomozygous57624316
3118627805118627806GGTT31GENIChomozygous57624318
3118627806118627807AATGTCATAACCTCTTTGTTAT31GENIChomozygous57624320
3118628269118628270GC25GENIChomozygous58015123
3118628695118628696AG36GENIChomozygous58015125
3118628946118628947TC18GENIChomozygous57624322
3118629610118629611TTTTTTTTTC15GENIChomozygous57624326
3118630173118630179ACACGC------19GENIChomozygous58015128
3118630221118630222GGCACA12GENIChomozygous58015131
3118630263118630264GGCA19GENICpossibly homozygous58015134