chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	3115678	3115679	C	T	35	GENIC	homozygous	114706174
6	3115724	3115725	A	G	33	GENIC	homozygous	115037008
6	3115726	3115727	G	A	32	GENIC	homozygous	118568314
6	3115727	3115728	A	G	30	GENIC	homozygous	118568316
6	3117516	3117517	G	C	19	GENIC	homozygous	114706175
6	3117878	3117879	G	T	19	GENIC	homozygous	115233099
6	3118197	3118198	G	T	22	GENIC	homozygous	118551928
6	3118311	3118312	T	A	30	GENIC	homozygous	114706180
6	3126128	3126129	G	A	17	GENIC	homozygous	115233109
6	3126130	3126131	T	G	15	GENIC	homozygous	115487950
6	3132559	3132560	C	G	22	GENIC	homozygous	114706189
6	3132580	3132581	G	C	16	GENIC	homozygous	114706190
6	3148316	3148317	C	A	23	GENIC	homozygous	118551930
6	3148333	3148334	C	T	21	GENIC	homozygous	114706226
6	3163144	3163145	T	C	17	GENIC	homozygous	118690051
6	3167251	3167252	G	A	14	GENIC	homozygous	118551933
6	3170200	3170201	T	A	17	GENIC	homozygous	114706254
6	3171070	3171071	G	A	26	GENIC	possibly homozygous	114706255
6	3173955	3173956	G	A	11	GENIC	homozygous	115037011
6	3174427	3174428	A	C	20	GENIC	homozygous	115037012
6	3174428	3174429	C	A	20	GENIC	homozygous	118551935
6	3181498	3181499	T	C	20	GENIC	homozygous	114706273
6	3181503	3181504	C	A	19	GENIC	homozygous	114706274