chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	116088837	116088838	G	T	13	GENIC	homozygous	140688009
X	116089419	116089420	T		12	GENIC	homozygous	140593761
X	116090391	116090392	G	A	7	GENIC	homozygous	140688010
X	116091707	116091708	G	A	4	GENIC	homozygous	140688011
X	116092156	116092157	C	A	7	GENIC	homozygous	140688012
X	116092581	116092581		T	11	GENIC	homozygous	140593762
X	116093595	116093596	G	C	9	GENIC	homozygous	140688013
X	116096050	116096051	T	C	11	GENIC	homozygous	140688014
X	116096149	116096149		A	2	GENIC	homozygous	140593765
X	116094491	116094492	A	G	2	GENIC	homozygous	148261013
X	116094492	116094493	T	A	2	GENIC	homozygous	148261014
X	116099364	116099365	G	T	12	GENIC	homozygous	140688015
X	116097078	116097082	CACC		2	GENIC	heterozygous	145100956
X	116103463	116103464	A		7	GENIC	homozygous	140593766
X	116106050	116106051	T	C	9	GENIC	homozygous	140688016
X	116108364	116108364		T	6	GENIC	homozygous	140593767
X	116112914	116112915	T	C	6	GENIC	homozygous	140688017
X	116113134	116113135	C	T	8	GENIC	homozygous	140688018