chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	10197604	10197605	C	T	30	GENIC	homozygous	108224077
X	10197807	10197808	T	C	26	GENIC	homozygous	108224079
X	10198567	10198568	A	G	31	GENIC	homozygous	108224081
X	10202919	10202920	C	T	24	GENIC	homozygous	108224083
X	10203452	10203453	T	C	30	GENIC	homozygous	108224085
X	10204481	10204482	G	A	30	GENIC	homozygous	108224087
X	10204650	10204651	G	A	27	GENIC	homozygous	108224089
X	10206555	10206556	G	T	24	GENIC	homozygous	108224091
X	10209075	10209076	A	G	31	GENIC	homozygous	108224093
X	10209267	10209268	G	A	34	GENIC	homozygous	108224095
X	10209681	10209682	G	A	32	GENIC	homozygous	108224097
X	10210001	10210002	C	T	29	GENIC	homozygous	108224101
X	10210828	10210829	G	A	30	GENIC	homozygous	108224103
X	10210844	10210845	C	G	30	GENIC	homozygous	108224105
X	10211934	10211935	A	T	30	GENIC	homozygous	108224107
X	10212151	10212152	C	T	27	GENIC	homozygous	108224112
X	10213116	10213117	T	C	25	GENIC	homozygous	108224114
X	10215609	10215610	C	T	18	GENIC	homozygous	108224116
X	10217771	10217772	A	G	35	GENIC	homozygous	108224118
X	10200178	10200179	T		26	GENIC	homozygous	129719527
X	10214963	10214965	GT		16	GENIC	homozygous	129719528
X	10215030	10215032	GT		20	GENIC	homozygous	129719529
X	10217809	10217809		A	37	GENIC	homozygous	129719530
X	10208660	10208661	C	T	21	GENIC	homozygous	108366661
X	10211315	10211316	G	A	35	GENIC	homozygous	108366663
X	10217176	10217177	A	G	25	GENIC	homozygous	108366665
X	10215053	10215114	GTGTGTGAGTGTGTGTGTGTGAGTGTGGTGTGTGTGTGAGTGAGGTGTGTGTGTCTGTGTG		22	GENIC	homozygous	135241293