chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	78359441	78359442	A	C	11	GENIC	homozygous	108276462
X	78365669	78365670	G	C	4	GENIC	homozygous	108276464
X	78370327	78370327		ATG	13	GENIC	heterozygous	129757849
X	78370345	78370346	T	C	15	GENIC	heterozygous	108276466
X	78370362	78370363	T	C	16	GENIC	heterozygous	108276468
X	78370370	78370371	A	G	16	GENIC	heterozygous	108276470
X	78376707	78376708	G	T	22	GENIC	homozygous	108276472
X	78379423	78379424	T	C	9	GENIC	homozygous	108276474
X	78379430	78379431	C		9	GENIC	homozygous	129757850
X	78381781	78381782	G	A	5	GENIC	homozygous	108276476
X	78386583	78386584	T		4	GENIC	homozygous	129757851
X	78386691	78386692	G	A	5	GENIC	heterozygous	119929492
X	78386754	78386755	C	T	2	GENIC	heterozygous	120003814
X	78386432	78386433	A	T	1	GENIC	homozygous	120030789
X	78386452	78386453	T	A	1	GENIC	homozygous	130509925
X	78386702	78386706	TGTT		5	GENIC	heterozygous	130499547
X	78387146	78387147	A	C	4	GENIC	heterozygous	120003818
X	78387547	78387548	C	T	2	GENIC	homozygous	120003819
X	78389077	78389078	T	C	4	GENIC	homozygous	119929494
X	78391681	78391682	T	C	11	GENIC	homozygous	108276478
X	78395353	78395354	A		9	GENIC	homozygous	129757853
X	78399514	78399515	G	A	11	GENIC	homozygous	108620134