chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141905243419052435AG16GENICpossibly homozygous48555028
141905313019053131A-2GENICheterozygous48555031
141905336019053361A-7GENICheterozygous48555033
141905365019053651AG13GENICheterozygous48555037
141905720319057204GT3GENIChomozygous48555066
141905720719057208AT2GENIChomozygous48555067
141905721619057217GT3GENIChomozygous49279030
141905721719057218AT3GENIChomozygous49279031
141905722019057221AG4GENIChomozygous48962335
141905722319057224CG2GENIChomozygous48962337
141905724719057248CG14GENICpossibly homozygous48555069
141905835519058356AAT3GENICheterozygous49279032
141905926019059261GA29GENICheterozygous49279033
141906132619061327CT25GENIChomozygous49279034
141906163319061634AG18GENICpossibly homozygous48555162
141906211919062120CA7GENICheterozygous48555169
141906456919064570GT4GENICheterozygous48555204
141906579019065791CT21GENIChomozygous48555216
141906604719066048CT18GENICpossibly homozygous49279035
141906641119066412CT26GENICheterozygous49279036
141906659919066600AT29GENICpossibly homozygous48555224