chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
37143636671436367GC19GENIChomozygous111606546
37143684571436846AG21GENIChomozygous111606549
37143783871437839TG29GENIChomozygous111606550
37144430271444303AT29GENIChomozygous111606553
37143853671438537CA23GENICpossibly homozygous119675082
37143859071438591AG19GENIChomozygous119675083
37143921871439219CT21GENICpossibly homozygous119675084
37144285871442859CT17GENICpossibly homozygous119732760
37144708071447081TA15GENICpossibly homozygous111922089
37144745771447458GT14GENIChomozygous111606555
37144746771447468AT15GENIChomozygous111606556
37144803171448032TG20GENIChomozygous111606557
37144870771448708CT18GENIChomozygous111922095
37145029971450300TG17GENICpossibly homozygous111922101
37144870971448710CT18GENIChomozygous120080855