chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103102367831023679CT26GENICpossibly homozygous116545422
103102425131024252TG21GENIChomozygous116545424
103102516131025162AT25GENICpossibly homozygous116545426
103102542731025428GT24GENIChomozygous116545428
103102901831029019TG24GENIChomozygous116545432
103103155231031553AC26GENICpossibly homozygous116545434
103103346031033461AG16GENIChomozygous116545440
103103675931036760TG20GENIChomozygous116545442
103103796931037970GC29GENIChomozygous116545444
103103844731038448GA33GENIChomozygous116545446
103104079931040800CG25GENIChomozygous116545448