chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121811393718113938AAC26GENIChomozygous684499613
121811672718116728AG49GENIChomozygous503618578
121811745318117454TC22GENIChomozygous505407810
121811749118117492GGT26GENIChomozygous684499614
121811749418117495G-27GENIChomozygous684499615
121811792618117927TA41GENICpossibly homozygous503618579
121811839518118396AAC52GENIChomozygous684499616
121811888318118884GA35GENIChomozygous503618580
121811929718119299GG--17GENIChomozygous684499617
121811989218119893AAT36GENIChomozygous684499618
121811990518119906TC39GENIChomozygous503618581
121812018018120181CCA56GENIChomozygous684499619
121812131518121316TG32GENICheterozygous505407811
121812220618122207CA39GENIChomozygous503618582
121812240618122407GA48GENICpossibly homozygous503618583
121812290118122902AG24GENIChomozygous503618584