chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	116059263	116059264	A	G	17	GENIC	homozygous	45200597
X	116059422	116059423	A	G	22	GENIC	possibly homozygous	45200598
X	116059954	116059955	A	C	1	GENIC	homozygous	45200599
X	116059964	116059968	AAAC	----	3	GENIC	heterozygous	45200600
X	116059975	116059976	C	A	6	GENIC	heterozygous	45200601
X	116060151	116060152	T	-	3	GENIC	heterozygous	45200603
X	116060377	116060378	T	TC	3	GENIC	heterozygous	45200605
X	116062524	116062525	G	GTGTA	8	GENIC	possibly homozygous	45200607
X	116063983	116063984	C	T	13	GENIC	homozygous	45200610
X	116064181	116064182	G	A	18	GENIC	possibly homozygous	45200611
X	116064252	116064253	T	C	18	GENIC	possibly homozygous	45200612
X	116064557	116064559	TA	--	3	GENIC	homozygous	45200613
X	116064742	116064743	C	T	14	GENIC	homozygous	45200614
X	116065151	116065152	A	ATG	1	GENIC	homozygous	45481652
X	116065808	116065953	AGAAGAGCAGCCAGTGGGGTTGGGGATTTAGCTCAGGGGGTTGGGGATTTAGCTCAGCGGTAGAGCACTTGCCTAGGGAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCCGGCAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAAA	-------------------------------------------------------------------------------------------------------------------------------------------------	4	GENIC	homozygous	45481654
X	116066042	116066043	A	G	7	GENIC	possibly homozygous	45200629
X	116066535	116066536	A	G	12	GENIC	homozygous	45200631
X	116066571	116066572	A	G	19	GENIC	possibly homozygous	45200632
X	116066645	116066646	G	A	11	GENIC	possibly homozygous	45200633
X	116067423	116067424	G	A	11	GENIC	homozygous	45200637
X	116067431	116067432	T	A	10	GENIC	homozygous	45200638