chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5155294274155294275CT19GENIChomozygous114064083
5155294360155294361TC12GENIChomozygous114064085
5155295748155295749TC22GENIChomozygous114064087
5155296213155296214TG28GENIChomozygous134554222
5155300981155300982TG35GENIChomozygous114064089
5155302190155302191GA14GENIChomozygous114064091
5155304171155304175CCCT2GENIChomozygous131856096
5155307760155307761AG23GENICpossibly homozygous114064093
5155308085155308086CT30GENIChomozygous114064095
5155308199155308200AC27GENIChomozygous114064097
5155308271155308272CT30GENIChomozygous114064099
5155308396155308397TC22GENIChomozygous114064101
5155308975155308976TC28GENIChomozygous114064103
5155309320155309321TG26GENIChomozygous114064105
5155309638155309639TG32GENIChomozygous114064107
5155309712155309713CT26GENIChomozygous114064109
5155311340155311341TC24GENIChomozygous114064111
5155311536155311537GC32GENIChomozygous114064113
5155311877155311878AG24GENIChomozygous114064115
5155311999155312000AG27GENICpossibly homozygous114064117
5155312352155312353AT29GENIChomozygous114064125
5155316261155316262TC25GENIChomozygous114064133
5155316409155316410AG25GENIChomozygous114064135
5155316472155316473TA25GENIChomozygous114064137
5155316661155316662CT38GENIChomozygous114064139
5155316675155316676TG34GENIChomozygous114064141
5155317165155317166TC33GENIChomozygous114064143
5155318171155318172CT26GENIChomozygous114064145
5155319466155319467GA24GENIChomozygous114064151
5155312305155312305CATGTGTGTATGTG32GENIChomozygous128261319
5155312166155312167G27GENIChomozygous128261318
5155315148155315149T25GENICpossibly homozygous128261320
5155316092155316096TGAA25GENIChomozygous128261321
5155305394155305394AGGAGCAGGACCCAGGACCAGGCCCTTTTCAGAGCCAGGGGACATTGTCATGAACTGAACTGCCC11GENIChomozygous128261315
5155307873155307874C31GENIChomozygous128261316
5155308852155308852T27GENIChomozygous128261317
5155318392155318393CT21GENIChomozygous114064147
5155318688155318689AG22GENIChomozygous114064149