chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	156658006	156658007	T	G	11	GENIC	possibly homozygous	71174635
5	156658011	156658012	T	G	10	GENIC	homozygous	71174637
5	156658016	156658017	T	G	14	GENIC	possibly homozygous	71174639
5	156658021	156658022	T	G	14	GENIC	homozygous	71174641
5	156666203	156666204	T	G	52	GENIC	heterozygous	71967710
5	156666215	156666216	T	G	63	GENIC	heterozygous	71967713
5	156666219	156666220	G	A	63	GENIC	heterozygous	71967716
5	156672825	156672826	G	A	25	GENIC	heterozygous	71967719
5	156672832	156672833	G	A	32	GENIC	heterozygous	71967722
5	156675500	156675501	C	G	33	GENIC	heterozygous	71967724
5	156677129	156677130	A	C	39	GENIC	heterozygous	71967727
5	156689000	156689001	A	G	35	GENIC	heterozygous	71174753
5	156709246	156709247	C	T	114	GENIC	heterozygous	71967730
5	156709248	156709249	G	T	113	GENIC	heterozygous	71967733
5	156709251	156709252	A	T	117	GENIC	heterozygous	71967736
5	156709256	156709257	T	G	116	GENIC	heterozygous	71967739
5	156709259	156709260	T	C	114	GENIC	heterozygous	71967742
5	156713287	156713288	G	T	29	GENIC	homozygous	71174809
5	156713750	156713751	T	G	53	GENIC	heterozygous	71967745
5	156713757	156713758	G	C	49	GENIC	heterozygous	71967748
5	156667323	156667324	T	G	25	GENIC	heterozygous	71470375
5	156729600	156729601	G	T	18	GENIC	heterozygous	71639145