chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	46153291	46153292	T	C	35	GENIC	homozygous	116585152
10	46154242	46154243	T	C	34	GENIC	homozygous	116585154
10	46154293	46154294	G	T	38	GENIC	homozygous	116585156
10	46154988	46154989	C	G	15	GENIC	homozygous	116585158
10	46156515	46156516	T	C	35	GENIC	homozygous	116585162
10	46157133	46157134	A	C	16	GENIC	homozygous	116585164
10	46157974	46157975	T	G	29	GENIC	homozygous	116585168
10	46160188	46160189	T	C	29	GENIC	homozygous	116585170
10	46161086	46161087	G	A	28	GENIC	homozygous	116585172
10	46161134	46161135	A	G	35	GENIC	homozygous	116585174
10	46161538	46161539	T	C	31	GENIC	homozygous	116585176
10	46163104	46163105	C	T	30	GENIC	homozygous	116585178
10	46163192	46163193	A	C	33	GENIC	homozygous	116585180
10	46165911	46165912	G	A	40	GENIC	homozygous	116585182
10	46166013	46166014	G	A	34	GENIC	homozygous	116585184
10	46167646	46167647	A	G	25	GENIC	homozygous	116585186
10	46168488	46168489	G	A	36	GENIC	homozygous	116585188
10	46171455	46171456	A	G	22	GENIC	homozygous	116585190