chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1224941916224941917CA43GENIChomozygous61100744
1224943475224943476GGT40GENIChomozygous61100745
1224943816224943818TT--30GENICheterozygous61100746
1224943817224943818T-30GENICheterozygous61100747
1224945369224945370CCTT4GENIChomozygous61100748
1224945611224945612TG53GENIChomozygous61100749
1224946008224946009CT68GENIChomozygous61100750
1224947183224947184GT53GENICpossibly homozygous61100751
1224948459224948460A-3GENICheterozygous61100752
1224948538224948539TA36GENICpossibly homozygous61100753
1224948726224948730CTTC----15GENIChomozygous61100754
1224948729224948730CT20GENICpossibly homozygous61100755
1224948933224948934CCT41GENICheterozygous61100756
1224948933224948934CCTT41GENICheterozygous61100757
1224950964224950965AAAAAC27GENIChomozygous61321488