chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3141577251141577252GA33GENIChomozygous112168817
3141577266141577267CA32GENIChomozygous112168819
3141577322141577323CT30GENIChomozygous112168821
3141577406141577407CT13GENIChomozygous112168823
3141577561141577562CA28GENIChomozygous112168825
3141577680141577681TA20GENIChomozygous112168827
3141577894141577895GA46GENIChomozygous111756242
3141578245141578246GA30GENIChomozygous112168829
3141578363141578364AC41GENIChomozygous111756246
3141578431141578432TA35GENIChomozygous111756248
3141578464141578465GC30GENIChomozygous111756250
3141578679141578680TC11GENIChomozygous111756256
3141578877141578878GA44GENIChomozygous112168831
3141579180141579181CT23GENIChomozygous111756258
3141579368141579369CT26GENIChomozygous111756260
3141579477141579478AT30GENIChomozygous112168833
3141581053141581054GA52GENIChomozygous112168835
3141581303141581304CT56GENIChomozygous111756268
3141582743141582744GT38GENIChomozygous111756274
3141582851141582852AG38GENIChomozygous112168837
3141583110141583111TC34GENIChomozygous111756275
3141583179141583180AG41GENICpossibly homozygous111756277
3141583447141583448AG64GENIChomozygous111756281
3141583801141583802AG24GENIChomozygous111756283
3141584610141584611TC49GENIChomozygous112168839
3141584674141584675TC30GENIChomozygous111756289
3141584689141584690CT27GENIChomozygous111756291
3141584706141584707CT19GENIChomozygous112168841
3141585155141585156AC28GENIChomozygous111756295
3141585881141585882CT28GENIChomozygous112168843
3141586682141586683CT38GENIChomozygous112168845
3141586715141586716AC29GENIChomozygous112168847
3141586795141586796AG14GENIChomozygous111756301
3141587552141587553TC21GENIChomozygous111756307
3141587821141587822AG35GENIChomozygous111756309
3141588826141588827GC36GENIChomozygous112168849
3141589200141589201CG36GENIChomozygous112168851
3141587013141587014TA8GENIChomozygous119685729