chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	2612393	2612394	A	G	21	GENIC	possibly homozygous	111516964
17	2614908	2614909	T	C	13	GENIC	possibly homozygous	111516966
17	2616807	2616808	G	A	21	GENIC	possibly homozygous	111516968
17	2618087	2618088	C	T	18	GENIC	homozygous	111516970
17	2626793	2626794	C	T	29	GENIC	possibly homozygous	111516973
17	2628977	2628978	G	A	31	GENIC	homozygous	111516975
17	2630262	2630263	A	G	25	GENIC	possibly homozygous	111516977
17	2631955	2631956	T	C	21	GENIC	possibly homozygous	111380065
17	2632597	2632598	C	T	23	GENIC	homozygous	111516979
17	2644588	2644589	A	C	32	GENIC	homozygous	111380071
17	2645619	2645620	C	A	25	GENIC	homozygous	111152767
17	2645643	2645644	A	C	19	GENIC	homozygous	111152769
17	2648471	2648472	C	T	27	GENIC	homozygous	111516981
17	2648692	2648693	T	A	19	GENIC	homozygous	111380073
17	2651518	2651519	A	T	25	GENIC	possibly homozygous	111516983
17	2652174	2652175	T	C	28	GENIC	possibly homozygous	111380078
17	2656246	2656247	A	C	15	GENIC	homozygous	110937225
17	2660022	2660023	C	T	24	GENIC	homozygous	111516985
17	2660601	2660602	T	C	9	GENIC	homozygous	111556003