chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	128156738	128156739	A	G	21	GENIC	homozygous	108331616
X	128156886	128156887	C	T	9	GENIC	homozygous	108331618
X	128164784	128164785	G	A	10	GENIC	homozygous	108331620
X	128165025	128165026	C	T	18	GENIC	homozygous	108331622
X	128174319	128174320	G	T	17	GENIC	homozygous	108331624
X	128176874	128176875	C	G	4	GENIC	homozygous	108331626
X	128184166	128184167	A	G	16	GENIC	homozygous	108331628
X	128189720	128189721	A	G	11	GENIC	homozygous	108331630
X	128193169	128193170	G	A	23	GENIC	homozygous	108331632
X	128195700	128195701	C	T	12	GENIC	homozygous	108331634
X	128197649	128197650	A	G	6	GENIC	homozygous	108331636
X	128206738	128206739	T	C	6	GENIC	homozygous	108331638
X	128207147	128207148	G	A	15	GENIC	homozygous	108331640
X	128209085	128209086	C	T	9	GENIC	homozygous	108331642
X	128211291	128211292	G	C	7	GENIC	homozygous	108331644
X	128211334	128211335	C	A	8	GENIC	homozygous	108331646
X	128214824	128214825	A	G	11	GENIC	homozygous	108331648
X	128237012	128237013	A	C	21	GENIC	homozygous	108331650
X	128241198	128241199	G	A	10	GENIC	homozygous	108331652
X	128241451	128241452	A	G	16	GENIC	homozygous	108331654
X	128243335	128243336	G	A	7	GENIC	homozygous	108331656
X	128243500	128243501	T	C	3	GENIC	homozygous	108331658
X	128251091	128251092	T	C	11	GENIC	homozygous	108331660
X	128252866	128252867	A	G	12	GENIC	homozygous	108331662
X	128253218	128253219	A	G	10	GENIC	homozygous	108331664
X	128254204	128254205	C	T	13	GENIC	homozygous	108331666
X	128258246	128258247	T	C	14	GENIC	homozygous	108331668
X	128258582	128258583	T	C	9	GENIC	homozygous	108331670
X	128259501	128259502	T	C	20	GENIC	homozygous	108331672
X	128260791	128260792	G	C	8	GENIC	homozygous	108331674
X	128264558	128264559	G	T	10	GENIC	homozygous	108331676
X	128265001	128265002	A	G	9	GENIC	homozygous	108331679