chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	167983445	167983446	C	T	33	GENIC	homozygous	114455484
5	167986869	167986870	A	C	34	GENIC	homozygous	114082916
5	167986930	167986931	G	A	30	GENIC	homozygous	114455486
5	167989641	167989642	C	A	39	GENIC	homozygous	114455487
5	167990590	167990591	T	C	35	GENIC	homozygous	114082922
5	167991620	167991621	A	G	27	GENIC	homozygous	114082923
5	167993959	167993960	G	C	24	GENIC	homozygous	114082927
5	167994044	167994045	C	T	29	GENIC	homozygous	114082928
5	167995107	167995108	C	T	39	GENIC	homozygous	114082929
5	167995253	167995254	G	A	41	GENIC	homozygous	114455488
5	167995371	167995372	T	C	31	GENIC	homozygous	114082931
5	167995418	167995419	T	C	34	GENIC	homozygous	114082932
5	167996710	167996711	C	G	26	GENIC	homozygous	114082934
5	167997804	167997805	G	A	30	GENIC	homozygous	114082935
5	167999302	167999303	G	A	24	GENIC	homozygous	114082936
5	167999633	167999634	A	T	25	GENIC	homozygous	114284397
5	168000088	168000089	T	C	19	GENIC	homozygous	114284399
5	168000923	168000924	T	C	28	GENIC	homozygous	114455489
5	168001729	168001730	T	A	21	GENIC	homozygous	114455491
5	168002026	168002027	C	T	31	GENIC	homozygous	114082943
5	168003162	168003163	C	T	24	GENIC	homozygous	114455493
5	168004368	168004369	G	A	9	GENIC	homozygous	119214139