chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2250293628250293629GA23GENIChomozygous110850139
2250294096250294097GA30GENIChomozygous110850141
2250294122250294123CG31GENIChomozygous110377850
2250294139250294140GA34GENIChomozygous110850143
2250295644250295645AC7GENIChomozygous110377856
2250296815250296816GC21GENIChomozygous110850145
2250297207250297208CT35GENIChomozygous110850147
2250297635250297636TC18GENIChomozygous110850149
2250297654250297655CT21GENIChomozygous110850152
2250297675250297676GT27GENIChomozygous110850154
2250298035250298036AG43GENIChomozygous110377858
2250298241250298242TC33GENIChomozygous110377860
2250298666250298667CT46GENICheterozygous110850159
2250298676250298677CT43GENICheterozygous110914983
2250298690250298691CA38GENICheterozygous110914985
2250298834250298835CT36GENIChomozygous110850161