chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	123910636	123910637	C	T	34	GENIC	possibly homozygous	45362460
X	123910729	123910730	C	G	13	GENIC	homozygous	45215164
X	123911775	123911795	CTATTTATTTATTTATTTAT	--------------------	7	GENIC	heterozygous	45215167
X	123911808	123911809	T	C	7	GENIC	heterozygous	45362461
X	123913077	123913078	A	T	15	GENIC	homozygous	45362465
X	123914006	123914007	T	C	24	GENIC	homozygous	45362467
X	123914069	123914070	G	T	23	GENIC	heterozygous	45440578
X	123914552	123914553	G	A	29	GENIC	homozygous	45362468
X	123916200	123916201	T	C	29	GENIC	homozygous	45215179
X	123916919	123916920	A	-	14	GENIC	homozygous	45215181
X	123918031	123918032	T	C	26	GENIC	possibly homozygous	45267667
X	123918237	123918238	G	A	35	GENIC	heterozygous	45215185
X	123918297	123918298	T	C	36	GENIC	heterozygous	45215186
X	123918814	123918815	G	A	23	GENIC	homozygous	45215187
X	123921046	123921050	ACAC	----	5	GENIC	heterozygous	45215188
X	123921048	123921050	AC	--	5	GENIC	heterozygous	45329170
X	123921793	123921794	C	T	5	GENIC	homozygous	45362469
X	123922091	123922094	GAG	---	3	GENIC	heterozygous	45215192
X	123922244	123922245	G	A	22	GENIC	possibly homozygous	45362470
X	123918866	123918867	A	G	20	GENIC	heterozygous	45314288
X	123922946	123922947	T	G	24	GENIC	possibly homozygous	45215195
X	123922950	123922951	T	G	24	GENIC	possibly homozygous	45215196
X	123922954	123922955	T	G	21	GENIC	heterozygous	45362471
X	123922975	123922976	C	T	19	GENIC	possibly homozygous	45215197
X	123922987	123922988	T	C	22	GENIC	heterozygous	45215200
X	123922991	123922992	T	C	22	GENIC	possibly homozygous	45215201
X	123924654	123924655	G	A	27	GENIC	possibly homozygous	45362472
X	123924766	123924767	G	A	24	GENIC	heterozygous	45362473
X	123925097	123925098	T	C	34	GENIC	homozygous	45215206