chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104592872145928722TC38GENIChomozygous142239733
104592881645928817CT44GENIChomozygous146956126
104592950845929509CT71GENIChomozygous146956127
104593213645932137AG54GENIChomozygous142239736
104593308345933084CT48GENIChomozygous146956128
104593598445935985AG43GENIChomozygous142239738
104593640245936403GC55GENIChomozygous142239739
104593641745936418CA54GENIChomozygous146956129
104593787845937879TG39GENIChomozygous142239740
104593797445937975GA48GENIChomozygous146956130
104593836345938364AG38GENIChomozygous146956131
104593841045938411CA48GENIChomozygous146956132
104593872345938724TC36GENIChomozygous142239741
104593922745939228CT45GENIChomozygous142239742
104593974945939750AG44GENIChomozygous146956133
104593975345939754AG45GENIChomozygous142239744
104593978245939783GA40GENIChomozygous142239745
104594005645940057CT43GENIChomozygous142239747
104594074445940745CT49GENIChomozygous146956134
104594181745941818TC43GENIChomozygous142239750
104594250245942503GA41GENIChomozygous145739785
104594271945942720CA48GENIChomozygous146956135
104594535045945351AC37GENIChomozygous142239757
104594694445946945CT34GENIChomozygous142239760
104593377245933773T10GENIChomozygous145729205
104593689745936897ATG48GENIChomozygous146935372
104593888745938887AAG29GENIChomozygous146935373
104594161945941619CCAACC55GENIChomozygous142201656
104594748245947483A40GENICpossibly homozygous146935374
104594920345949204TC58GENIChomozygous142239762