chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124905139449051395CA10GENICpossibly homozygous50230926
124905236449052365AT11GENIChomozygous50230932
124905276849052769TC22GENICpossibly homozygous50230934
124905539549055396AC10GENIChomozygous50230936
124905566749055668GGA2GENICheterozygous50230938
124905572249055723TG3GENICheterozygous50513695
124905614649056147CA6GENIChomozygous50230942