chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	13263155	13263156	G	A	37	GENIC	homozygous	108228644
X	13265226	13265227	T	C	31	GENIC	homozygous	108228646
X	13265360	13265361	T	C	30	GENIC	homozygous	108228648
X	13265745	13265746	T	C	41	GENIC	homozygous	108228650
X	13265888	13265889	G	C	42	GENIC	homozygous	119903602
X	13266136	13266137	T	C	43	GENIC	homozygous	108228652
X	13266156	13266157	A	G	50	GENIC	homozygous	108228654
X	13267425	13267426	A	G	48	GENIC	homozygous	108228656
X	13267587	13267588	T	C	56	GENIC	homozygous	108228658
X	13268424	13268425	G	A	44	GENIC	homozygous	108228660
X	13271499	13271500	G	C	16	GENIC	homozygous	119903604
X	13271582	13271583	C	T	38	GENIC	possibly homozygous	108523441
X	13272075	13272076	G	A	43	GENIC	homozygous	108228662
X	13272518	13272519	G	C	48	GENIC	homozygous	108228664
X	13272804	13272805	T	G	52	GENIC	homozygous	108228666
X	13273948	13273949	G	A	63	GENIC	homozygous	108228668
X	13274729	13274730	C	T	41	GENIC	homozygous	108228670
X	13275763	13275764	C	T	51	GENIC	homozygous	120046613
X	13277273	13277274	T	C	35	GENIC	homozygous	108228672
X	13277500	13277501	G	A	39	GENIC	homozygous	108228674
X	13278375	13278376	C	A	40	GENIC	homozygous	108228676
X	13279365	13279366	G	T	32	GENIC	homozygous	108228678
X	13279500	13279501	G	A	43	GENIC	homozygous	108228680
X	13279777	13279778	C	T	37	GENIC	possibly homozygous	108228682
X	13280415	13280416	T	C	21	GENIC	homozygous	108730255
X	13281244	13281245	T	G	31	GENIC	homozygous	108438928
X	13281418	13281419	A	G	43	GENIC	homozygous	108228684
X	13281455	13281456	A	C	41	GENIC	possibly homozygous	108228686
X	13281877	13281878	A	C	37	GENIC	homozygous	108228688
X	13281961	13281962	G	T	36	GENIC	possibly homozygous	108228690
X	13282023	13282024	C	A	33	GENIC	homozygous	108228692
X	13282125	13282126	G	A	39	GENIC	homozygous	108228694