chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	160175313	160175314	A	G	42	GENIC	homozygous	114160561
5	160175334	160175335	G	A	41	GENIC	homozygous	114160562
5	160175639	160175640	C	T	39	GENIC	homozygous	114160563
5	160175689	160175690	G	A	41	GENIC	homozygous	114160564
5	160175712	160175713	C	T	47	GENIC	homozygous	114160565
5	160175801	160175802	A	C	43	GENIC	homozygous	114160566
5	160175943	160175944	T	G	55	GENIC	homozygous	114160567
5	160175958	160175959	G	A	55	GENIC	homozygous	114160568
5	160175975	160175976	A	G	58	GENIC	homozygous	114160569
5	160176018	160176019	T	C	57	GENIC	homozygous	114160570
5	160176397	160176398	A	G	69	GENIC	possibly homozygous	114160571
5	160176809	160176810	A	G	63	GENIC	homozygous	114160572
5	160176821	160176822	A	T	63	GENIC	homozygous	114160573
5	160176836	160176837	A	G	68	GENIC	homozygous	114160574
5	160177294	160177295	C	T	46	GENIC	homozygous	114160575
5	160177640	160177641	G	A	29	GENIC	homozygous	114160576
5	160177642	160177643	C	A	29	GENIC	homozygous	114160577
5	160177866	160177866		CTGA	49	GENIC	homozygous	130964182
5	160177896	160177897	T	C	54	GENIC	homozygous	114160578
5	160178257	160178258	C	T	62	GENIC	homozygous	114160579
5	160178581	160178582	T	C	33	GENIC	homozygous	114160580
5	160178601	160178602	C	G	37	GENIC	homozygous	114160581
5	160178745	160178746	A	G	53	GENIC	homozygous	114160582
5	160178846	160178846		T	51	GENIC	homozygous	130964183
5	160178894	160178895	G	C	60	GENIC	homozygous	114160583
5	160179022	160179023	T	C	58	GENIC	homozygous	114160584
5	160179232	160179233	A	G	69	GENIC	homozygous	114160585
5	160179918	160179919	T	C	64	GENIC	homozygous	114160586