chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3160554458160554459TC80GENIChomozygous111793012
3160554762160554763GA53GENIChomozygous111793014
3160554901160554902CA62GENICpossibly homozygous111793016
3160555097160555098CG54GENIChomozygous111793018
3160555683160555684TC48GENIChomozygous111793020
3160556035160556036AG56GENIChomozygous111793022
3160556580160556581CT52GENIChomozygous111793024
3160557164160557165CG40GENIChomozygous111793026
3160557191160557192AG44GENICpossibly homozygous111793028
3160557335160557336AG53GENICpossibly homozygous111793030
3160557732160557733GA37GENICheterozygous111793032
3160557735160557736CT34GENICheterozygous111793034
3160557738160557739CG36GENICheterozygous111793036
3160557744160557745TC37GENICheterozygous111793038
3160557830160557831TC38GENIChomozygous111793040
3160558259160558260TC58GENICpossibly homozygous111793042
3160558799160558800GA60GENICpossibly homozygous111793044
3160560814160560815TC49GENIChomozygous111793046