chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
58053546980535470GA12GENICpossibly homozygous55490388
58053597680535977GA6GENICheterozygous55490392
58053617480536175GA20GENIChomozygous55490394
58053826880538269CT15GENICpossibly homozygous55490396
58053977580539777TT--2GENIChomozygous55490398
58054068480540685CG11GENICheterozygous55490400
58054083380540834GA12GENIChomozygous55490402
58054440180544402CT23GENIChomozygous55490406
58054825580548256CT29GENIChomozygous55490412
58054869380548694CT4GENIChomozygous55490414
58054912980549133TTTG----7GENIChomozygous55490416
58055538080555381AG27GENICpossibly homozygous55490424
58055551480555515CT24GENICpossibly homozygous55490426
58055900780559008CT12GENIChomozygous55490430
58056033980560341AT--1GENIChomozygous55490464
58056057480560575GT21GENIChomozygous55490468
58056186280561863CT2GENIChomozygous55490472