chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
31395125113951252CT24GENIChomozygous58494827
31395172613951727TC7GENIChomozygous57161275
31395210413952105CA11GENIChomozygous59999345
31395251713952518AG17GENIChomozygous57161283
31395541113955418TTTTTTT-------5GENIChomozygous59999346
31395582113955823AC--14GENIChomozygous57161298
31395594213955943CCA6GENICheterozygous58276201
31395603013956031GC17GENIChomozygous57161301
31395616013956161AAAG6GENICheterozygous58540227
31395616113956162AAG6GENICheterozygous58571256
31395616713956168AAG7GENICheterozygous58571257
31395617013956171GA7GENICheterozygous58540229
31395644713956449AA--12GENICheterozygous57161309
31395644813956449A-12GENICheterozygous57161312
31395669913956700CCGCAGGCAG2GENIChomozygous57161320
31395678813956789AG17GENIChomozygous57161323
31395758413957585TC13GENIChomozygous57161330
31395865313958654GGCACACGCACGCA6GENIChomozygous59999347
31395871113958712GA18GENIChomozygous57161350
31395884313958844CT17GENIChomozygous59999348
31395914013959141TTA6GENICheterozygous57161368
31395925813959259AC21GENIChomozygous57161370
31396027413960276GT--14GENIChomozygous58494829
31396163413961635CCA11GENICheterozygous58637572
31396201113962012T-8GENIChomozygous58540231
31396201313962045TCATAAAAACATAAAATAAAAATAAATGAAAT--------------------------------22GENICpossibly homozygous58540233
31396332813963329AAT18GENICheterozygous59921661
31396385113963852TG19GENIChomozygous57161410
31396392113963922GA20GENIChomozygous59999349
31396397013963971CCTGCT19GENIChomozygous59999350
31396404013964041T-14GENICheterozygous57867706
31396509513965096CA26GENIChomozygous58494831
31396662413966641TGTTTTTCAGCCAATAC-----------------17GENICheterozygous58679340
31396185513961859TTTT----8GENIChomozygous58664976