chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85378074753780748TC21GENIChomozygous675070858
85378121053781211AG18GENIChomozygous675070859
85378128853781289A-20GENIChomozygous771157298
85378193153781932TTTTA1GENIChomozygous771157303
85378200853782013GTTTG-----17GENIChomozygous771157305
85378241353782414CT32GENIChomozygous675070860
85378321953783220CT36GENICpossibly homozygous675070861
85378331953783320AG26GENIChomozygous675070862
85378348153783482CT30GENIChomozygous675070863
85378360953783610TC25GENIChomozygous675070864
85378373853783739GT37GENIChomozygous675070865
85378379353783794TC22GENIChomozygous675070866
85378391053783922GTGTGTGTGTGC------------7GENICheterozygous771157306
85378404853784049TC25GENIChomozygous675070867
85378408953784090T-18GENICpossibly homozygous771157307
85378629253786293TTAC6GENICheterozygous771157309
85378713253787133CG23GENIChomozygous675070868