chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	2625516	2625517	A	C	23	GENIC	heterozygous	119982319
X	2625560	2625561	C	T	20	GENIC	heterozygous	119982321
X	2625779	2625780	G	T	24	GENIC	heterozygous	119900322
X	2626114	2626115	C	G	24	GENIC	heterozygous	119900324
X	2626403	2626404	G	A	28	GENIC	heterozygous	120064238
X	2627307	2627308	A	C	8	GENIC	heterozygous	119900325
X	2633049	2633050	G	A	30	GENIC	possibly homozygous	119900326
X	2633079	2633080	T	G	28	GENIC	heterozygous	119900327
X	2629410	2629411	T	C	14	GENIC	homozygous	108437245
X	2630547	2630548	A	C	6	GENIC	homozygous	108216777
X	2630930	2630931	T	G	16	GENIC	homozygous	108216779
X	2632318	2632319	A	G	12	GENIC	homozygous	108216783
X	2632591	2632592	A	G	5	GENIC	homozygous	108216785
X	2631609	2631610	A	C	5	GENIC	homozygous	108363197
X	2635170	2635171	C	T	15	GENIC	homozygous	108216787
X	2635521	2635522	C	T	45	GENIC	heterozygous	119900329
X	2635552	2635553	G	A	55	GENIC	heterozygous	119900330
X	2635556	2635557	G	A	56	GENIC	heterozygous	119900331
X	2635570	2635571	C	G	56	GENIC	heterozygous	119900332
X	2640302	2640303	A	T	103	GENIC	heterozygous	119900334
X	2641495	2641496	C	A	5	GENIC	homozygous	108216789
X	2642278	2642279	G	A	12	GENIC	homozygous	108216791
X	2643123	2643124	G	A	14	GENIC	homozygous	108216793
X	2644027	2644028	G	A	9	GENIC	homozygous	108216795
X	2646719	2646720	T	G	16	GENIC	homozygous	108216797
X	2650382	2650383	A	C	5	GENIC	homozygous	108216799
X	2650582	2650583	T	A	10	GENIC	heterozygous	108216802
X	2651280	2651281	A	G	6	GENIC	homozygous	108216804
X	2651923	2651924	G	A	8	GENIC	homozygous	108216806
X	2652186	2652187	A	T	14	GENIC	homozygous	108216808
X	2653352	2653353	T	C	10	GENIC	homozygous	108216810