chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	1321796	1321797	T	G	8	GENIC	homozygous	125139401
X	1321808	1321809	A	G	5	GENIC	homozygous	125139402
X	1322012	1322013	T	C	19	GENIC	homozygous	125097974
X	1323389	1323390	T	C	25	GENIC	homozygous	125097975
X	1325105	1325106	T	C	23	GENIC	homozygous	108215902
X	1326954	1326955	C	T	16	GENIC	homozygous	108215905
X	1330884	1330885	C	A	15	GENIC	heterozygous	108437065
X	1341620	1341621	C	T	10	GENIC	homozygous	108215910
X	1341880	1341881	A	C	12	GENIC	homozygous	125097976
X	1347555	1347556	A	G	8	GENIC	homozygous	108215912
X	1359254	1359255	A	G	17	GENIC	homozygous	108215915
X	1359573	1359574	G	C	10	GENIC	homozygous	108215917
X	1363254	1363255	G	A	20	GENIC	homozygous	108215920
X	1364203	1364204	A	G	20	GENIC	homozygous	108215922
X	1364687	1364688	T	A	24	GENIC	homozygous	108215925
X	1367236	1367237	G	A	25	GENIC	homozygous	108215927
X	1369400	1369401	A	C	13	GENIC	homozygous	108215930
X	1369986	1369987	T	C	22	GENIC	homozygous	108215932
X	1372912	1372913	C	T	30	GENIC	homozygous	108215934
X	1374983	1374984	G	A	26	GENIC	homozygous	108215937