chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104427180844271809CT34GENIChomozygous116769295
104427227844272279GA36GENIChomozygous118081871
104427329044273291AG19GENIChomozygous117008164
104427515044275151TC25GENIChomozygous116769381
104427585444275855AT34GENIChomozygous118081872
104427769944277700CT19GENIChomozygous116769433
104427850244278503TC30GENICpossibly homozygous116769447
104427909844279099TC40GENIChomozygous116769457
104428141444281415AC33GENIChomozygous116580984
104428245944282460CT36GENIChomozygous118081873
104428266044282661AG32GENIChomozygous116769617