chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	30004852	30004853	G	GT	9	GENIC	heterozygous	45629316
X	30031541	30031544	ATT	---	1	GENIC	homozygous	45117101
X	30035668	30035670	TG	--	7	GENIC	heterozygous	45505207
X	30043016	30043018	CA	--	3	GENIC	heterozygous	45505209
X	30053199	30053244	AGAAGGCAAATTCTTGATTTGGGCTATTCTTCAAATCCTCAAAGA	---------------------------------------------	1	GENIC	homozygous	45505211
X	30070560	30070561	G	GT	18	GENIC	homozygous	45117103
X	30047061	30047062	G	GA	7	GENIC	homozygous	45679707
X	30073890	30073891	G	-	7	GENIC	heterozygous	45586468
X	30087492	30087493	T	-	4	GENIC	homozygous	45117105
X	30090278	30090279	A	-	24	GENIC	homozygous	45117107
X	30091367	30091368	T	TCTGCTGCTGCTGCTACTGCTGTTGTTGTTGCTGCTACTGCTGTTGCTGCTGCTGCTGCTGCTACTGCTACTGCTGTTGCTG	3	GENIC	homozygous	45505213
X	30099480	30099482	TG	--	9	GENIC	homozygous	45505215
X	30107725	30107727	AC	--	6	GENIC	heterozygous	45505217
X	30113983	30113984	C	CGCTTGCCTAGCAAGCA	8	GENIC	homozygous	45505221
X	30115968	30115969	T	TTAC	6	GENIC	heterozygous	45788564
X	30136162	30136163	A	ACT	2	GENIC	homozygous	45505225