chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4183022663183022664GGA29GENIChomozygous733112437
4183024349183024350TC27GENIChomozygous608744226
4183024366183024367GA26GENIChomozygous608744227
4183024727183024728CCAAAA18GENICheterozygous733112439
4183026259183026260TTACAC11GENICpossibly homozygous733112441
4183026660183026661CT25GENIChomozygous608744228
4183027418183027420AA--21GENIChomozygous733112442
4183028012183028013TC25GENICpossibly homozygous608744229
4183028022183028023GA25GENIChomozygous608744230
4183029418183029419GA33GENIChomozygous608744231
4183030153183030154GGTGA24GENIChomozygous733112444
4183030392183030393CT20GENIChomozygous608744232
4183030662183030663CT30GENIChomozygous608744233
4183030673183030674AG28GENIChomozygous608744234
4183032232183032233AC24GENIChomozygous608744235
4183032311183032312GT17GENIChomozygous608744236
4183032618183032619AG19GENIChomozygous608744237
4183033099183033103AAAA----3GENIChomozygous733112445
4183033102183033103AACC3GENIChomozygous733112447
4183033554183033555CT10GENIChomozygous608744238
4183033622183033623AT10GENICpossibly homozygous606108457
4183035208183035211AAA---15GENIChomozygous733112449
4183035223183035224AG18GENIChomozygous608744239
4183036184183036185TC25GENIChomozygous608744240
4183036319183036333GTGTGTGTGTGTGT--------------13GENIChomozygous733112451
4183036708183036709TC14GENIChomozygous608744241
4183037103183037104GT24GENIChomozygous606108458
4183037269183037270GA20GENIChomozygous608744242
4183037794183037795TC18GENIChomozygous608744243
4183037949183037950TG16GENIChomozygous606108459
4183038145183038146GA22GENIChomozygous608744244
4183039836183039837TA29GENIChomozygous606108460
4183040348183040349CT17GENIChomozygous608744245