chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141572302515723026AG22GENIChomozygous139459017
141572333815723339AT20GENIChomozygous139459020
141572335515723356CT22GENIChomozygous146552459
141572351815723519CT25GENIChomozygous146552460
141572389315723894CG10GENIChomozygous146552461
141572389515723896CG9GENIChomozygous146552462
141572389715723898CG9GENIChomozygous146552463
141572389915723900CG9GENIChomozygous146552464
141572390115723902CG9GENIChomozygous146552465
141572402215724023GA12GENIChomozygous146552466
141572409715724098AG14GENIChomozygous146552467
141572433815724338TC11GENIChomozygous146546702
141572447815724478T21GENIChomozygous146546703
141572464315724644GA7GENIChomozygous146552468
141572468415724684AA4GENIChomozygous146546704
141572478315724784TC17GENIChomozygous139459021
141572485115724852AT28GENIChomozygous146552469
141572504115725042CT24GENIChomozygous146552470
141572519415725195TA21GENIChomozygous139459022
141572549615725497TC12GENIChomozygous139459023
141572565315725654TG6GENIChomozygous139459024
141572576715725768TG8GENIChomozygous146552471
141572584415725854ATATGTATAA4GENIChomozygous146546705
141572643915726440AT16GENICpossibly homozygous146552472