chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
14815194848151949TA26GENIChomozygous60699204
14815250248152503AG34GENIChomozygous60699205
14815272948152730TC33GENIChomozygous60699206
14815295548152956TC32GENIChomozygous60699207
14815317048153172CT--30GENIChomozygous60699208
14815324348153244GA27GENIChomozygous60699209
14815344748153448AG27GENIChomozygous60699210
14815505648155057TA50GENICpossibly homozygous60699211
14815681148156812GA19GENIChomozygous60699212
14815732048157321TC33GENICpossibly homozygous60699213
14815735448157475AAAACAACAGAAGAGGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCGCAAGGCTCTGGGTTCGGTCCCCAGCTCCGAAAAAAAAGAACCAAAAAAAAAAAAAAAAAAA-------------------------------------------------------------------------------------------------------------------------38GENICpossibly homozygous62074883
14815755948157570CCCTCAAAACC-----------30GENIChomozygous60699214
14815757548157576G-27GENIChomozygous60699215
14815775748157758CCCTGCAGTTCTCCTCCTGCAGTACCCCTCCTGCAGTGCCCCTT9GENIChomozygous62365113
14815781148157812CCT17GENIChomozygous60699220
14815813848158139AG34GENIChomozygous60699221
14815824148158242CT36GENIChomozygous60699222
14815841548158416CA37GENIChomozygous60699223
14815848248158483TC36GENIChomozygous60699224
14815854548158546AAACACTC19GENIChomozygous60699225
14815871548158723ACTTGTGC--------32GENICpossibly homozygous60699226
14815893448158935AG19GENICpossibly homozygous60699227
14815898848158989CT15GENIChomozygous60699228
14815902948159030AG20GENIChomozygous60699229
14815926948159270GA32GENIChomozygous60699230
14815967148159672G-31GENIChomozygous60699231
14815970948159710AG31GENIChomozygous60699232
14815975248159753AC23GENIChomozygous60699233
14815976848159769GT21GENIChomozygous60699234