chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124933065649330657TC25GENIChomozygous115348885
124933080249330803TC19GENIChomozygous115348887
124933100249331003GA25GENIChomozygous115348889
124933124249331243TC28GENIChomozygous115348893
124933192449331925CT21GENIChomozygous115348895
124933244549332446CT14GENIChomozygous115348897
124933327049333271AC25GENIChomozygous115348899
124933399649333997AG23GENIChomozygous115348901
124933443249334433CG21GENIChomozygous115348903
124933485749334858GA25GENIChomozygous115348905
124933535049335351TG16GENIChomozygous115348907
124933685149336852CT17GENIChomozygous115348911
124933685249336853AG18GENIChomozygous115348913
124933744849337449AG30GENIChomozygous115348915
124933813749338138GT19GENIChomozygous115348917
124933939449339395GC26GENIChomozygous115348919
124933944649339447CG23GENICpossibly homozygous115348921
124934005049340051TC17GENIChomozygous115348923
124934100049341001TC11GENICpossibly homozygous115348925
124934121049341211CT20GENIChomozygous115348927
124936981049369811GA20GENIChomozygous115348929
124937002449370025CT21GENIChomozygous115444345
124937260649372607GA15GENIChomozygous115348931
124937301749373018AG32GENIChomozygous115348933
124937654149376542AG17GENIChomozygous115348935
124937827749378278GA18GENIChomozygous118274174
124937823749378238TC14GENIChomozygous118274171
124937825649378257TC13GENICheterozygous118274172
124937825749378258GA13GENICheterozygous118274173
124937828249378283AT18GENICheterozygous118274175
124937834349378344AT16GENIChomozygous118274176
124937837149378372GA17GENICheterozygous118274177
124938684949386850AG17GENICpossibly homozygous115348937
124939490949394910GA27GENIChomozygous115444346
124938153049381531CA31GENIChomozygous115480685
124938154249381543AC27GENIChomozygous115521758
124938155049381551CA27GENICpossibly homozygous115521759