chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
119016814690168147TG32GENIChomozygous50863212
119016901290169026TATTACCCCCAACC--------------20GENIChomozygous50863213
119017008890170089AG34GENIChomozygous50863214
119017110390171104AG22GENIChomozygous50863215
119017128590171286CCA18GENICpossibly homozygous50863216
119017136390171364TC29GENIChomozygous50863217
119017207590172076AG31GENIChomozygous50863218
119017232890172329GGAAAAA6GENICheterozygous51192855
119017232890172329GGAAAA6GENICheterozygous51197683
119017244490172445CT18GENIChomozygous50863222