chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
173068142930681429A16GENIChomozygous129442254
173068971330689714G29GENIChomozygous129442255
173069103630691037T21GENIChomozygous129442256
173069126630691266A13GENICpossibly homozygous129442257
173069288430692885TG16GENIChomozygous111023397
173068668730686688CT22GENIChomozygous111023387
173068748430687485TC29GENIChomozygous111023389
173068799830687999TC20GENIChomozygous111023391
173068818530688186CG22GENIChomozygous111023393
173069174630691747CG11GENIChomozygous111023395
173069428730694288G19GENIChomozygous129442258
173069444130694441T11GENIChomozygous129442259
173069444530694445T11GENIChomozygous129442260
173069447230694472T7GENIChomozygous129442262
173069448030694481G7GENIChomozygous129442263
173069459930694600TC19GENIChomozygous111023399
173069490830694909AG21GENIChomozygous111023401
173069492730694928CT19GENIChomozygous111023403
173069868530698686TG27GENIChomozygous111023405
173069985630699857TC13GENIChomozygous111344869
173070034430700348AAAT17GENIChomozygous129442264
173070055530700556AG21GENIChomozygous111023407
173070153230701533TA31GENIChomozygous111023409
173070193630701937GT17GENIChomozygous111023411
173070260130702602TC25GENIChomozygous111023413
173070278330702784AG15GENIChomozygous111023415
173070289830702899GA17GENIChomozygous111023417
173069676930696770AG16GENIChomozygous111499390
173070336930703370GA33GENIChomozygous111023419
173070507430705075A22GENIChomozygous129442265
173070686230706863TC24GENIChomozygous111023421
173070878330708784GT21GENIChomozygous111023423
173070957330709574T18GENIChomozygous129442266
173071003230710032T8GENICheterozygous131529295
173071222630712227CT29GENIChomozygous111023431
173070962630709627CT12GENIChomozygous111023425
173070992330709924AG18GENIChomozygous111023427
173071138930711390CT21GENIChomozygous111023429
173071230930712310A37GENIChomozygous129442267