chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
314894391489440AG32GENICpossibly homozygous111428224
314900061490007AG28GENICpossibly homozygous111428227
314919401491941GA21GENICpossibly homozygous119960123
314933591493360CT38GENICpossibly homozygous111428230
314942531494254AT26GENICpossibly homozygous111428234
314946561494657AG27GENICpossibly homozygous111428237
314982151498216TC40GENIChomozygous111428252
314994111499412GA26GENIChomozygous119960125
314994751499476CT24GENIChomozygous119960127
315018731501874AT26GENICpossibly homozygous119960129
315030301503031GC20GENICpossibly homozygous111428261
315051391505140CA31GENIChomozygous111428263
315053211505322AC30GENIChomozygous111428264
315053251505326TC28GENIChomozygous111428265
315055741505575AG27GENICpossibly homozygous111428266
315119141511915CT24GENIChomozygous119960133
315119541511955GA24GENIChomozygous119960135
315120311512032TC31GENICpossibly homozygous119960137
315126881512689AG29GENIChomozygous119960139
315134131513414TG30GENIChomozygous119960141
315136591513660CG32GENICpossibly homozygous119960143
315144761514477TC16GENIChomozygous119960149
315146681514669GA21GENICpossibly homozygous119960151