chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1224941822224941823CG20GENIChomozygous61926278
1224943816224943818TT--20GENICheterozygous61100746
1224943817224943818T-20GENICheterozygous61100747
1224945369224945370CCTT4GENICheterozygous61100748
1224945611224945612TG27GENIChomozygous61100749
1224946008224946009CT31GENIChomozygous61100750
1224947183224947184GT31GENIChomozygous61100751
1224948933224948934CCTT29GENICheterozygous61100757
1224945369224945370CCT4GENICheterozygous62355242
1224948474224948475AAAGAG11GENIChomozygous62102827
1224948726224948727CCT11GENICpossibly homozygous62249933
1224950964224950965AAAAACAAACAAAC25GENIChomozygous62249934