chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8118556574118556577TCT---36GENICheterozygous695931002
8118556577118556578GGGC41GENICheterozygous695931003
8118556578118556583TCTGT-----41GENICheterozygous695931004
8118556691118556692GA61GENIChomozygous534765088
8118556845118556846AG58GENIChomozygous534765089
8118557229118557230GGA13GENICheterozygous695931005
8118557231118557232AAACTGAATATCAGGGAT22GENIChomozygous695931006
8118557553118557554GA37GENIChomozygous537084158
8118557615118557617AC--26GENICheterozygous695931007
8118557617118557618A-27GENICheterozygous695931008
8118557618118557620CC--11GENICpossibly homozygous695931009
8118557881118557882AG53GENIChomozygous537084159
8118557936118557937AATT35GENIChomozygous695931010
8118557968118557969AG31GENIChomozygous537084160
8118558134118558135TG29GENIChomozygous534765090
8118558151118558152CT28GENIChomozygous537084161
8118558191118558192AG25GENIChomozygous537084162
8118558202118558203CT23GENICheterozygous537084163
8118558233118558234CG21GENIChomozygous537084164
8118558340118558341AG31GENIChomozygous534765091
8118558364118558365GGC31GENIChomozygous695931011
8118558460118558461TC39GENIChomozygous534765092
8118558497118558498AG46GENIChomozygous534765093
8118558560118558561GGAC40GENIChomozygous695931012
8118558729118558730AG39GENIChomozygous534765094
8118558744118558745CA41GENIChomozygous534765095
8118558987118558988AC38GENIChomozygous534765096
8118559066118559096TACAGTTAATGTTTACGTTATTTGCACGTA------------------------------6GENIChomozygous695931013
8118559355118559356AG39GENIChomozygous534765097
8118559501118559502TC44GENIChomozygous537084165
8118559559118559560TC43GENIChomozygous537084166
8118559642118559643TG58GENIChomozygous537084167
8118559741118559742TG42GENIChomozygous534765098
8118559823118559824CCATAA13GENICpossibly homozygous695931014
8118559950118559951GA45GENIChomozygous537084168
8118560021118560022CT46GENIChomozygous534765099