chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
81128000511280006AC22GENIChomozygous142034254
81128087811280879TC21GENIChomozygous142034255
81128487411284875CT10GENIChomozygous142034256
81128487511284876AG10GENIChomozygous142034257
81128567611285677CT20GENIChomozygous142034258
81128740111287402GC23GENIChomozygous142034259
81128771711287718AG22GENIChomozygous142034260
81128776411287765CT24GENIChomozygous142034261
81128913311289134GA22GENIChomozygous142034262
81128944511289446CT16GENIChomozygous142034263
81128987211289873AG17GENIChomozygous142034264
81129120111291202AG32GENIChomozygous142034265
81129157711291578CT21GENIChomozygous142034266
81129226611292267GA11GENIChomozygous142034267
81129353211293533CT24GENIChomozygous142034268
81129543711295438GA21GENIChomozygous142034269
81129859411298604GGTGAGGTGA9GENIChomozygous142016924
81128640311286404T21GENIChomozygous142016920
81129493211294933A12GENIChomozygous142016921
81129520811295208C10GENIChomozygous142016922
81129559811295598A13GENIChomozygous142016923
81129928011299320GGTGAGGTGAGGTGAGGTGAGGTGAGGTGAGGTGCGGTGA10GENICpossibly homozygous142016927
81130055011300551C15GENIChomozygous142016928
81130117111301175ATGT20GENIChomozygous142016929
81130145411301455T18GENIChomozygous142016930
81130326511303266T22GENIChomozygous142016931
81130371111303712CT26GENIChomozygous142034270
81130412911304130GT16GENIChomozygous142034271
81130443211304433AG16GENIChomozygous142034272
81130445011304451GA17GENIChomozygous142034273
81129908011299125GGTGCGGTGCGGTGAGGTGAGGTGAGGTGAGGTGAGGTGAGGTGC2GENICheterozygous147848973