chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	104816449	104816450	A	G	23	GENIC	homozygous	149194753
X	104868361	104868361		AG	11	GENIC	homozygous	140590809
X	104875742	104875744	GT		5	GENIC	heterozygous	145100742
X	104868431	104868432	A	G	11	GENIC	homozygous	147331368
X	104887699	104887700	A		11	GENIC	homozygous	140590811
X	104897785	104897786	T		14	GENIC	heterozygous	145162323
X	104920003	104920004	T	C	25	GENIC	heterozygous	140674815
X	104920170	104920171	C	T	39	GENIC	heterozygous	140674816
X	104920590	104920591	T	G	14	GENIC	heterozygous	149194754
X	104920571	104920572	A	T	15	GENIC	heterozygous	404451693
X	104868431	104868432	A		11	GENIC	heterozygous	403782885
X	104982611	104982612	T	C	12	GENIC	heterozygous	149194755
X	104982615	104982616	A	T	11	GENIC	heterozygous	149194756
X	105076602	105076603	C	A	10	GENIC	homozygous	403485584
X	105076602	105076603	C		10	GENIC	heterozygous	403485585
X	104983190	104983191	C		11	GENIC	heterozygous	149193924
X	105011284	105011285	C	T	22	GENIC	heterozygous	141065544
X	105011303	105011304	A	C	22	GENIC	heterozygous	141065545
X	105019643	105019644	G	C	22	GENIC	homozygous	148243394
X	105068493	105068493		AC	7	GENIC	possibly homozygous	141061791
X	105076594	105076596	AA		7	GENIC	heterozygous	141061792