chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	123913702	123913703	C	CA	5	GENIC	heterozygous	45362466
X	123916918	123916919	G	GA	6	GENIC	homozygous	45388260
X	123918237	123918238	G	A	17	GENIC	heterozygous	45215185
X	123918297	123918298	T	C	17	GENIC	heterozygous	45215186
X	123918814	123918815	G	A	7	GENIC	homozygous	45215187
X	123921764	123921765	A	G	6	GENIC	homozygous	45388262
X	123921793	123921794	C	T	4	GENIC	homozygous	45362469
X	123922136	123922138	AG	--	5	GENIC	homozygous	45388264
X	123922433	123922434	G	A	9	GENIC	homozygous	45388266
X	123922830	123922831	A	G	8	GENIC	homozygous	45215194
X	123922938	123922939	G	T	4	GENIC	homozygous	45388268
X	123922942	123922943	G	T	4	GENIC	homozygous	45388270
X	123922975	123922976	C	T	5	GENIC	heterozygous	45215197
X	123922987	123922988	T	C	6	GENIC	heterozygous	45215200
X	123922991	123922992	T	C	6	GENIC	heterozygous	45215201
X	123923014	123923015	T	C	8	GENIC	heterozygous	45388272
X	123923089	123923090	C	G	12	GENIC	homozygous	45388274
X	123923491	123923492	G	A	3	GENIC	homozygous	45388275
X	123923495	123923502	AGTGTCG	-------	1	GENIC	homozygous	45388277
X	123923725	123923726	G	T	10	GENIC	homozygous	45388279
X	123923842	123923843	G	GA	9	GENIC	homozygous	45388281
X	123924253	123924254	T	C	7	GENIC	homozygous	45388283
X	123924310	123924311	C	T	10	GENIC	homozygous	45388285
X	123925097	123925098	T	C	9	GENIC	homozygous	45215206