chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	53092266	53092267	C	T	17	GENIC	homozygous	111063009
17	53092309	53092310	G	C	6	GENIC	homozygous	111063010
17	53092446	53092447	C	G	10	GENIC	homozygous	111063011
17	53092843	53092844	G	A	28	GENIC	homozygous	111063012
17	53093051	53093052	A	G	42	GENIC	homozygous	111063013
17	53093136	53093137	A	G	23	GENIC	homozygous	111063014
17	53093425	53093426	A	G	5	GENIC	homozygous	111063016
17	53093555	53093556	T	C	17	GENIC	homozygous	111063017
17	53093569	53093570	C	T	20	GENIC	homozygous	111063018
17	53093619	53093620	C	T	26	GENIC	homozygous	111063019
17	53093936	53093937	C	T	18	GENIC	homozygous	111063021
17	53093937	53093938	G	A	18	GENIC	homozygous	111063022
17	53094177	53094178	A	C	17	GENIC	homozygous	111063023
17	53095299	53095300	G	A	23	GENIC	homozygous	111063024
17	53095441	53095442	T	C	18	GENIC	homozygous	111063025
17	53095917	53095918	C	T	52	GENIC	homozygous	111063026
17	53096968	53096969	G	A	11	GENIC	homozygous	111063027
17	53097026	53097027	C	T	11	GENIC	homozygous	111063028
17	53097376	53097377	T	C	20	GENIC	homozygous	111063029
17	53097836	53097837	C	T	22	GENIC	homozygous	111063030
17	53098685	53098686	A	T	40	GENIC	homozygous	111063031
17	53098762	53098763	C	T	35	GENIC	homozygous	111063032
17	53096031	53096032	A	T	12	GENIC	homozygous	111530335
17	53099728	53099729	A	C	6	GENIC	homozygous	111530337