chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	113607298	113607299	A	G	20	GENIC	homozygous	108310889
X	113614340	113614341	T	C	13	GENIC	homozygous	108715935
X	113616437	113616438	G	A	20	GENIC	homozygous	108715937
X	113620997	113620998	A	C	7	GENIC	possibly homozygous	108310961
X	113620998	113620999	A	C	7	GENIC	possibly homozygous	108310963
X	113623538	113623539	C	T	22	GENIC	homozygous	108715939
X	113624573	113624574	A	G	15	GENIC	homozygous	108715941
X	113626698	113626699	C	T	14	GENIC	homozygous	108715943
X	113639080	113639081	C	T	4	GENIC	homozygous	108715945
X	113642082	113642083	C	A	19	GENIC	homozygous	108311039
X	113643509	113643510	T	C	17	GENIC	homozygous	108715947
X	113644005	113644006	T	C	13	GENIC	homozygous	108577200
X	113646019	113646020	G	A	12	GENIC	homozygous	108311041
X	113648451	113648452	A	G	19	GENIC	homozygous	108311043
X	113649584	113649585	G	A	20	GENIC	homozygous	108453905
X	113649816	113649817	G	A	15	GENIC	homozygous	108311048
X	113650162	113650163	G	A	12	GENIC	homozygous	108311050
X	113650767	113650768	G	A	21	GENIC	homozygous	108311052
X	113650883	113650884	A	T	20	GENIC	homozygous	108311054
X	113651005	113651006	C	T	17	GENIC	homozygous	108311056
X	113651074	113651075	T	C	16	GENIC	homozygous	108311058
X	113651595	113651596	C	T	19	GENIC	homozygous	108311060
X	113652052	113652053	A	T	15	GENIC	homozygous	108311063
X	113652139	113652140	T	C	11	GENIC	homozygous	108311065
X	113653745	113653746	T	G	10	GENIC	homozygous	108311073
X	113653767	113653768	A	C	10	GENIC	homozygous	108311075
X	113653778	113653779	A	G	8	GENIC	homozygous	108311077
X	113655461	113655462	C	T	20	GENIC	homozygous	108453907
X	113655503	113655504	T	A	23	GENIC	homozygous	108715949