chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	77875489	77875495	TCTCTG	------	8	GENIC	homozygous	45668597
X	77876212	77876213	C	-	10	GENIC	homozygous	45152510
X	77880013	77880014	G	GAT	6	GENIC	homozygous	45152513
X	77880014	77880015	G	GA	8	GENIC	homozygous	45152515
X	77882387	77882388	A	AGGGGAAGGAGG	17	GENIC	homozygous	45152517
X	77882428	77882429	C	CA	17	GENIC	homozygous	45152518
X	77883513	77883514	T	G	8	GENIC	homozygous	45152519
X	77884965	77884966	G	A	10	GENIC	homozygous	45152520
X	77886016	77886020	AGCC	----	1	GENIC	homozygous	45695927
X	77886256	77886257	T	TTTGTTTTTGC	8	GENIC	homozygous	45152526
X	77886451	77886452	A	T	9	GENIC	homozygous	45152527
X	77887983	77887984	C	-	9	GENIC	homozygous	45152528
X	77890629	77890630	T	C	14	GENIC	homozygous	45152529
X	77892079	77892080	T	TAGACAGAC	15	GENIC	homozygous	45152530
X	77893513	77893514	G	A	19	GENIC	homozygous	45152531