chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	78359861	78359862	C	T	5	GENIC	homozygous	108392420
X	78360948	78360949	C	T	2	GENIC	homozygous	108686038
X	78363444	78363445	T	G	4	GENIC	homozygous	108392422
X	78368545	78368546	G	A	4	GENIC	homozygous	108392424
X	78370255	78370256	C	T	22	GENIC	heterozygous	119929489
X	78370290	78370291	T	G	32	GENIC	heterozygous	108686044
X	78370345	78370346	T	C	38	GENIC	heterozygous	108276466
X	78370362	78370363	T	C	32	GENIC	heterozygous	108276468
X	78370493	78370494	A	G	17	GENIC	heterozygous	119929490
X	78370500	78370501	G	A	18	GENIC	heterozygous	120003808
X	78370759	78370760	A	G	13	GENIC	possibly homozygous	108686046
X	78371912	78371913	G	A	7	GENIC	homozygous	108392426
X	78370370	78370371	A	G	28	GENIC	heterozygous	108276470
X	78376707	78376708	G	T	15	GENIC	homozygous	108276472
X	78381781	78381782	G	A	11	GENIC	homozygous	108276476
X	78391454	78391455	G	A	2	GENIC	homozygous	108392430
X	78393168	78393169	T	A	6	GENIC	heterozygous	108392432
X	78398333	78398334	T	C	7	GENIC	heterozygous	108686048
X	78388994	78388995	T	C	8	GENIC	heterozygous	108596578