chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	111800677	111800678	C	G	12	GENIC	heterozygous	131248940
X	111800685	111800686	C	T	12	GENIC	heterozygous	131248941
X	111800693	111800694	C	T	12	GENIC	heterozygous	131248942
X	111800696	111800697	T	A	12	GENIC	heterozygous	131248943
X	111800732	111800733	A	T	11	GENIC	heterozygous	131248944
X	111800800	111800801	T	A	7	GENIC	heterozygous	131248945
X	111800812	111800813	T	G	6	GENIC	heterozygous	120059959
X	111800967	111800968	C	T	5	GENIC	heterozygous	131248946
X	111801015	111801016	T	C	6	GENIC	heterozygous	131248947
X	111801016	111801017	T	C	6	GENIC	heterozygous	131248948
X	111801081	111801082	A	G	7	GENIC	heterozygous	130202206