chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
167612268176122682CT18GENICpossibly homozygous139986950
167612298476122985AG31GENIChomozygous139986951
167612310576123106AG23GENICpossibly homozygous139986952
167612530576125306GA24GENIChomozygous139986953
167612584976125850GA19GENIChomozygous139986954
167612617276126173CT20GENIChomozygous139986955
167612868876128689CA24GENIChomozygous139986956
167612882276128823CA18GENIChomozygous139986957
167613280876132809CT23GENIChomozygous139986958
167613411976134121AA14GENIChomozygous139846381
167613412276134144GAAGGAAGGAAGGAAGGAAGGA14GENIChomozygous139846382
167613423876134238AGAGAGAGAGA14GENICheterozygous149505601