chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	37190015	37190019	ACAC	----	1	GENIC	homozygous	45125055
X	37202729	37202730	A	-	19	GENIC	homozygous	45125056
X	37204893	37204894	C	CCT	17	GENIC	heterozygous	45125057
X	37204916	37204917	T	TCC	14	GENIC	heterozygous	45125058
X	37209412	37209413	C	G	35	GENIC	heterozygous	45125059
X	37209553	37209554	T	G	26	GENIC	heterozygous	45125060
X	37209722	37209723	C	G	38	GENIC	heterozygous	45125061
X	37209757	37209758	G	T	36	GENIC	heterozygous	45125062
X	37217716	37217717	T	C	40	GENIC	heterozygous	45125063
X	37217742	37217743	G	A	43	GENIC	heterozygous	45125064
X	37217743	37217744	T	C	43	GENIC	heterozygous	45125065
X	37217752	37217753	G	A	42	GENIC	heterozygous	45125066
X	37217807	37217808	G	T	48	GENIC	heterozygous	45125067
X	37220374	37220375	C	T	37	GENIC	heterozygous	45125068
X	37220382	37220383	G	A	37	GENIC	heterozygous	45125069
X	37230431	37230435	AGAG	----	5	GENIC	heterozygous	45125070
X	37230433	37230435	AG	--	5	GENIC	heterozygous	45125071
X	37232409	37232410	A	AG	2	GENIC	homozygous	45125072
X	37232426	37232427	A	G	9	GENIC	heterozygous	45125073
X	37232434	37232435	A	G	11	GENIC	heterozygous	45125074
X	37232440	37232441	T	TG	5	GENIC	heterozygous	45125075
X	37232508	37232509	C	T	48	GENIC	heterozygous	45125076
X	37232513	37232514	T	C	51	GENIC	heterozygous	45125077
X	37232531	37232532	G	A	45	GENIC	heterozygous	45125078
X	37232532	37232533	G	A	44	GENIC	heterozygous	45125079
X	37232565	37232566	A	G	36	GENIC	heterozygous	45125080
X	37232581	37232582	G	-	21	GENIC	heterozygous	45125081
X	37235722	37235723	T	C	27	GENIC	heterozygous	45125082
X	37235726	37235727	C	G	30	GENIC	heterozygous	45125083
X	37235728	37235729	T	A	28	GENIC	heterozygous	45125084
X	37235758	37235759	T	A	36	GENIC	heterozygous	45125085
X	37235771	37235772	A	T	35	GENIC	heterozygous	45125086
X	37235879	37235880	C	G	69	GENIC	heterozygous	45125087
X	37235896	37235897	A	C	70	GENIC	heterozygous	45125088