chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3118618615118618616CT57GENIChomozygous57624280
3118618660118618661AG66GENIChomozygous57624282
3118618668118618669AC70GENIChomozygous57624284
3118619117118619125TTTTTTTT--------7GENICheterozygous58015097
3118619118118619125TTTTTTT-------7GENICheterozygous58015100
3118621248118621249CG59GENIChomozygous57624288
3118621367118621368CT50GENIChomozygous57624290
3118621810118621811AT61GENIChomozygous58015103
3118621834118621835GA57GENIChomozygous58015106
3118622991118622992GA36GENICpossibly homozygous58015109
3118623022118623024TT--2GENICheterozygous58015112
3118623023118623024T-2GENICheterozygous57624296
3118623043118623044CT41GENICheterozygous58015115
3118623568118623569AG47GENIChomozygous57624298
3118624227118624228GGCACA6GENIChomozygous57624302
3118626819118626820T-36GENIChomozygous58015117
3118626820118626821G-21GENIChomozygous57624308
3118627098118627106AAACAAAC--------18GENIChomozygous58015120
3118627804118627805CCT22GENIChomozygous57624316
3118627805118627806GGTT10GENIChomozygous57624318
3118627806118627807AATGTCATAACCTCTTTGTTAT12GENIChomozygous57624320
3118628269118628270GC46GENIChomozygous58015123
3118628695118628696AG51GENIChomozygous58015125
3118628946118628947TC60GENIChomozygous57624322
3118629610118629611TTTTTTTTTC20GENIChomozygous57624326
3118630173118630179ACACGC------28GENIChomozygous58015128
3118630221118630222GGCA12GENICheterozygous57624328
3118630221118630222GGCACA12GENICheterozygous58015131
3118630263118630264GGCA24GENIChomozygous58015134