chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	115021215	115021216	A	G	14	GENIC	possibly homozygous	45726839
X	115022643	115022644	A	G	18	GENIC	possibly homozygous	45198328
X	115022676	115022677	T	C	9	GENIC	possibly homozygous	45920513
X	115022694	115022695	C	T	8	GENIC	heterozygous	45198329
X	115023411	115023412	T	C	23	GENIC	homozygous	45920514
X	115023642	115023643	T	G	25	GENIC	possibly homozygous	45198331
X	115023945	115023946	A	G	9	GENIC	possibly homozygous	45198332
X	115023994	115023995	T	C	2	GENIC	homozygous	45198333
X	115024772	115024773	C	T	6	GENIC	heterozygous	45920516
X	115026417	115026418	C	A	11	GENIC	homozygous	45920517
X	115027601	115027602	G	T	11	GENIC	homozygous	45920518
X	115028126	115028127	G	A	28	GENIC	possibly homozygous	45920519
X	115028303	115028304	C	T	17	GENIC	possibly homozygous	45920520
X	115031584	115031585	G	A	7	GENIC	heterozygous	45198364
X	115033610	115033611	A	G	10	GENIC	homozygous	45198367
X	115034008	115034009	G	-	3	GENIC	heterozygous	45920522
X	115035179	115035180	T	C	9	GENIC	homozygous	45198369
X	115037371	115037372	A	AAG	12	GENIC	homozygous	45198375
X	115037602	115037605	CCA	---	10	GENIC	homozygous	45920526
X	115043250	115043251	A	G	23	GENIC	homozygous	45198378
X	115043322	115043323	A	G	8	GENIC	homozygous	45198379
X	115051445	115051446	C	T	16	GENIC	possibly homozygous	45198385
X	115053265	115053266	C	T	29	GENIC	possibly homozygous	45920527
X	115053712	115053713	T	C	16	GENIC	homozygous	45198388
X	115054153	115054154	G	A	28	GENIC	possibly homozygous	45920528
X	115055417	115055418	G	GCCT	6	GENIC	heterozygous	45920529