chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7138088747138088748AG28GENIChomozygous55881007
7138088868138088869AG22GENIChomozygous55881009
7138089383138089384GA31GENIChomozygous55881011
7138090363138090364AT30GENIChomozygous55881013
7138091014138091015G-34GENIChomozygous55881015
7138091413138091414TTAA15GENICheterozygous54140924
7138091413138091414TTA15GENICpossibly homozygous54140925
7138093555138093556GGGTGTGTGTGTGTGTGT1GENIChomozygous55060256
7138094405138094406CT30GENIChomozygous55881017
7138095123138095124TC38GENIChomozygous54140946
7138095183138095184GT40GENIChomozygous55881019
7138095479138095480CT31GENIChomozygous55881021
7138095651138095652CCAA18GENICheterozygous54140949
7138095651138095652CCAAAAAAAAAA18GENICheterozygous54924019
7138095866138095867GA31GENIChomozygous55881023
7138096042138096043AG42GENIChomozygous54140950
7138096232138096233AC28GENIChomozygous54140951
7138096705138096706A-24GENIChomozygous54140952
7138096841138096843GT--32GENIChomozygous55881025
7138096864138096865CCGT34GENIChomozygous55881027
7138096897138096905GTGTGTAC--------25GENICpossibly homozygous55881029
7138096923138096927GTGT----8GENIChomozygous55881031
7138098077138098078TC36GENIChomozygous54140961
7138098203138098204GA31GENIChomozygous54140962
7138098866138098867AG38GENIChomozygous54140964
7138099043138099044GA26GENIChomozygous55881033
7138099173138099174GA39GENIChomozygous54140965
7138099452138099453CT34GENIChomozygous54140966
7138099545138099546CCT26GENIChomozygous55881035
7138099578138099579AG35GENICpossibly homozygous54140967
7138100413138100414CT33GENIChomozygous55881037
7138099486138099487AG25GENIChomozygous55314931