chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	53092266	53092267	C	T	20	GENIC	homozygous	111063009
17	53092309	53092310	G	C	20	GENIC	homozygous	111063010
17	53092446	53092447	C	G	28	GENIC	homozygous	111063011
17	53092843	53092844	G	A	23	GENIC	homozygous	111063012
17	53093051	53093052	A	G	30	GENIC	homozygous	111063013
17	53093136	53093137	A	G	37	GENIC	homozygous	111063014
17	53093392	53093393	A	C	34	GENIC	homozygous	111063015
17	53093425	53093426	A	G	29	GENIC	homozygous	111063016
17	53093555	53093556	T	C	30	GENIC	homozygous	111063017
17	53093569	53093570	C	T	29	GENIC	homozygous	111063018
17	53093619	53093620	C	T	37	GENIC	homozygous	111063019
17	53093655	53093656	A	G	30	GENIC	homozygous	111063020
17	53094177	53094178	A	C	25	GENIC	homozygous	111063023
17	53094762	53094763	G	C	20	GENIC	heterozygous	119293260
17	53094769	53094770	G	A	22	GENIC	heterozygous	111352328
17	53094778	53094779	C	T	22	GENIC	heterozygous	119293261
17	53094797	53094798	G	A	24	GENIC	heterozygous	119293262
17	53094836	53094837	C	T	20	GENIC	heterozygous	119293263
17	53095299	53095300	G	A	21	GENIC	homozygous	111063024
17	53095441	53095442	T	C	18	GENIC	homozygous	111063025
17	53095917	53095918	C	T	35	GENIC	homozygous	111063026
17	53096968	53096969	G	A	32	GENIC	possibly homozygous	111063027
17	53097026	53097027	C	T	19	GENIC	homozygous	111063028
17	53097376	53097377	T	C	23	GENIC	homozygous	111063029
17	53097836	53097837	C	T	17	GENIC	homozygous	111063030
17	53098667	53098668	A	G	47	GENIC	heterozygous	119293265
17	53098685	53098686	A	T	43	GENIC	possibly homozygous	111063031
17	53098762	53098763	C	T	29	GENIC	homozygous	111063032
17	53100366	53100367	A	G	30	GENIC	homozygous	111063033