chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1101680730101680731TA29GENIChomozygous60779879
1101686240101686241CCT3GENICheterozygous62350435
1101697440101697441AG8GENIChomozygous60779882
1101699595101699596TTGGTG18GENIChomozygous62085353
1101699599101699603AACA----19GENIChomozygous62147176
1101699654101699655C-19GENIChomozygous60779883
1101711593101711597ACAC----8GENICheterozygous62245695
1101711595101711597AC--8GENICheterozygous62229262
1101712944101712945TG27GENICpossibly homozygous60779888
1101716939101716940TTGGGGATTTAGCTCAGTGGTAGAGCGCTTGCCTAGCAAGCA7GENIChomozygous62147178
1101734960101734961T-24GENIChomozygous60779892
1101736162101736163A-4GENICheterozygous61299543