chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4148139718148139719CG16GENIChomozygous112875231
4148139928148139929AG16GENIChomozygous112875232
4148141709148141710CG29GENIChomozygous112875233
4148141884148141885GT21GENIChomozygous112875234
4148142073148142074GT18GENIChomozygous112875235
4148146850148146851GA30GENIChomozygous112875236
4148148599148148600TC19GENIChomozygous112875237
4148158745148158746GA22GENIChomozygous112875249
4148159220148159221TC34GENIChomozygous112875250
4148159373148159374TC23GENIChomozygous112875251
4148159882148159883AT22GENIChomozygous112875252
4148161423148161424AC17GENIChomozygous112875254
4148161628148161629CT27GENIChomozygous112875255
4148161637148161638TC24GENIChomozygous112875256
4148163030148163031CA18GENICpossibly homozygous112875257
4148164919148164920CT35GENIChomozygous112875273
4148165648148165649CT12GENIChomozygous112875274
4148165973148165974TC31GENIChomozygous112875275
4148166376148166377GA26GENIChomozygous112875276
4148167142148167143GA20GENIChomozygous112875277
4148167196148167197TA21GENIChomozygous112875278
4148169217148169218AT17GENIChomozygous112875279
4148171703148171704AG26GENIChomozygous112875285
4148173644148173645GC29GENIChomozygous112875286
4148173663148173664CA25GENIChomozygous112875287
4148173674148173675GA25GENIChomozygous112875288
4148173676148173677CT24GENIChomozygous112875289
4148173705148173706GA25GENIChomozygous112875290
4148173713148173714GA23GENIChomozygous112875291
4148173758148173759GA15GENIChomozygous112875292
4148173772148173773CT19GENIChomozygous112875293
4148173778148173779CT20GENIChomozygous112875294
4148174098148174099GA27GENIChomozygous112875295
4148174779148174780TC15GENIChomozygous112875297
4148185838148185839GA34GENIChomozygous112875299
4148188853148188854GA24GENIChomozygous112875300
4148189894148189895CT18GENIChomozygous112875301
4148194035148194036TC33GENIChomozygous112875302
4148197127148197128CA21GENIChomozygous112875303