chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	29421485	29421485		G	22	GENIC	homozygous	140580535
X	29423298	29423299	T	C	15	GENIC	homozygous	140631552
X	29424414	29424415	T	C	19	GENIC	homozygous	140631553
X	29434133	29434134	G	A	20	GENIC	homozygous	140631554
X	29434424	29434425	C	T	22	GENIC	homozygous	140631555
X	29436296	29436297	G		22	GENIC	heterozygous	141101065
X	29437574	29437574		C	32	GENIC	homozygous	140580536
X	29437845	29437846	A	C	15	GENIC	homozygous	140631556
X	29440068	29440069	A	T	26	GENIC	homozygous	140631557
X	29441958	29441958		TA	10	GENIC	homozygous	140580537
X	29449679	29449679		A	17	GENIC	homozygous	140580538
X	29451474	29451475	T	C	22	GENIC	homozygous	140631558
X	29451801	29451802	G	A	24	GENIC	homozygous	140631559
X	29452088	29452092	TGTG		6	GENIC	homozygous	140933002
X	29452471	29452472	T	C	19	GENIC	homozygous	140631560
X	29456507	29456508	G		22	GENIC	homozygous	140580539
X	29456892	29456893	G	T	18	GENIC	homozygous	140631561
X	29457574	29457575	G	A	28	GENIC	homozygous	140631562
X	29460737	29460738	T	C	4	GENIC	homozygous	140631563
X	29461171	29461172	G	A	21	GENIC	homozygous	140631564
X	29462409	29462410	A		31	GENIC	homozygous	140580540
X	29462943	29462944	C	T	23	GENIC	homozygous	140631565
X	29466727	29466728	C	T	21	GENIC	homozygous	140631566
X	29467808	29467809	G	C	24	GENIC	homozygous	140631567