chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2264787421264787422AC51GENIChomozygous110442216
2264789374264789375AG21GENIChomozygous110442217
2264789445264789446AG19GENICpossibly homozygous110442218
2264790609264790610GA30GENIChomozygous110442219
2264791645264791646TA16GENIChomozygous110442220
2264796843264796844CA18GENIChomozygous110442221
2264797353264797354TC21GENIChomozygous110442222
2264799277264799278CA21GENIChomozygous110442223
2264801244264801245TA39GENIChomozygous110442224
2264805817264805818GA31GENIChomozygous110442225
2264807499264807500AC17GENIChomozygous110442226
2264810614264810615TA19GENIChomozygous110442227
2264811817264811818CA50GENICpossibly homozygous110442228
2264817003264817004TC41GENIChomozygous110442229
2264819819264819820CT67GENIChomozygous110442230
2264825757264825758AG58GENIChomozygous110442231
2264828502264828503TC45GENIChomozygous110442232
2264829503264829504TA36GENIChomozygous110442233
2264831586264831587CT12GENIChomozygous110442234
2264832967264832968GA17GENIChomozygous110442235