chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	1321532	1321533	T	A	16	GENIC	homozygous	108437056
X	1321565	1321566	C	T	16	GENIC	homozygous	108523088
X	1321798	1321799	A	C	24	GENIC	homozygous	108215890
X	1321810	1321811	T	C	26	GENIC	homozygous	108215893
X	1322014	1322015	A	G	22	GENIC	homozygous	108215896
X	1323391	1323392	A	G	17	GENIC	homozygous	108215899
X	1325105	1325106	T	C	7	GENIC	homozygous	108215902
X	1326954	1326955	C	T	9	GENIC	homozygous	108215905
X	1329239	1329240	C	A	26	GENIC	possibly homozygous	108215907
X	1330884	1330885	C	A	5	GENIC	homozygous	108437065
X	1331731	1331732	T	C	21	GENIC	heterozygous	120045721
X	1341620	1341621	C	T	4	GENIC	homozygous	108215910
X	1347555	1347556	A	G	6	GENIC	heterozygous	108215912
X	1359254	1359255	A	G	4	GENIC	homozygous	108215915
X	1359573	1359574	G	C	13	GENIC	homozygous	108215917
X	1363254	1363255	G	A	7	GENIC	homozygous	108215920
X	1364203	1364204	A	G	27	GENIC	homozygous	108215922
X	1364687	1364688	T	A	14	GENIC	homozygous	108215925
X	1367236	1367237	G	A	8	GENIC	homozygous	108215927
X	1369400	1369401	A	C	13	GENIC	homozygous	108215930
X	1369986	1369987	T	C	15	GENIC	homozygous	108215932
X	1372912	1372913	C	T	20	GENIC	homozygous	108215934
X	1374983	1374984	G	A	19	GENIC	homozygous	108215937
X	1347738	1347739	T	A	4	GENIC	homozygous	119899352