chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101300117413001175GA19GENIChomozygous568548171
101300118313001184TTAC20GENICpossibly homozygous708754897
101300124813001249GGCACACACACA2GENIChomozygous708754900
101300165413001678TTCTTTCTTTCTTTCTTTCTTTCT------------------------8GENIChomozygous708754901
101300370513003706GGAC12GENIChomozygous708754903
101300380413003805GGA4GENICheterozygous708754904
101300416313004164CT21GENIChomozygous568548172
101300429613004297TTCTCTCACACACACACA14GENICpossibly homozygous708754907
101300472713004728CT18GENIChomozygous566741072
101300546013005461TC22GENIChomozygous566741073
101300652613006527GGACCGACCA3GENIChomozygous708754910