chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	160175313	160175314	A	G	23	GENIC	homozygous	114160561
5	160175334	160175335	G	A	26	GENIC	homozygous	114160562
5	160175639	160175640	C	T	27	GENIC	homozygous	114160563
5	160175801	160175802	A	C	32	GENIC	homozygous	114160566
5	160175943	160175944	T	G	29	GENIC	homozygous	114160567
5	160175958	160175959	G	A	29	GENIC	homozygous	114160568
5	160175975	160175976	A	G	33	GENIC	homozygous	114160569
5	160176018	160176019	T	C	43	GENIC	homozygous	114160570
5	160176397	160176398	A	G	34	GENIC	homozygous	114160571
5	160176809	160176810	A	G	37	GENIC	homozygous	114160572
5	160176821	160176822	A	T	37	GENIC	homozygous	114160573
5	160176836	160176837	A	G	39	GENIC	homozygous	114160574
5	160177294	160177295	C	T	39	GENIC	homozygous	114160575
5	160177640	160177641	G	A	32	GENIC	homozygous	114160576
5	160177642	160177643	C	A	32	GENIC	homozygous	114160577
5	160177896	160177897	T	C	32	GENIC	homozygous	114160578
5	160178257	160178258	C	T	29	GENIC	homozygous	114160579
5	160178894	160178895	G	C	26	GENIC	homozygous	114160583
5	160179022	160179023	T	C	39	GENIC	homozygous	114160584
5	160179232	160179233	A	G	26	GENIC	homozygous	114160585
5	160179918	160179919	T	C	30	GENIC	homozygous	114160586