chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
162104794621047947TC16GENICpossibly homozygous47993037
162104901021049011TTCACACACA3GENICheterozygous47741289
162104901121049013CA--3GENICheterozygous47993038
162104929621049297T-1GENIChomozygous47882589
162104979221049793AG30GENIChomozygous47993040
162105057721050578CT9GENIChomozygous47993041
162105375821053759AACTG7GENICpossibly homozygous47329460
162105482721054828CT15GENICpossibly homozygous47993042
162105792721057928TC4GENIChomozygous48166147
162105891321058914C-3GENIChomozygous47329484
162106460721064608GC15GENIChomozygous47993046
162106545321065454A-3GENICheterozygous47993047
162107297321072974TC4GENIChomozygous47993049
162107314121073142GA17GENICpossibly homozygous47993050
162107413821074139GA15GENIChomozygous47993051
162107440521074406TG3GENICheterozygous47993053
162107440621074407TG3GENICheterozygous48166148
162107441821074421TTT---4GENICheterozygous47993054
162107546021075461GA17GENICpossibly homozygous47993055
162107548921075490CT18GENICpossibly homozygous47993056
162107805421078055GA13GENIChomozygous47993057