chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	115022643	115022644	A	G	13	GENIC	homozygous	45198328
X	115022694	115022695	C	T	18	GENIC	heterozygous	45198329
X	115023319	115023320	G	C	19	GENIC	homozygous	45198330
X	115023642	115023643	T	G	21	GENIC	possibly homozygous	45198331
X	115023945	115023946	A	G	15	GENIC	possibly homozygous	45198332
X	115023994	115023995	T	C	2	GENIC	heterozygous	45198333
X	115025069	115025070	A	G	5	GENIC	homozygous	45198352
X	115028217	115028218	G	T	22	GENIC	possibly homozygous	45198355
X	115028525	115028526	T	C	14	GENIC	homozygous	45198361
X	115028611	115028612	G	A	6	GENIC	homozygous	45198362
X	115029541	115029542	A	G	9	GENIC	homozygous	45198363
X	115031584	115031585	G	A	7	GENIC	homozygous	45198364
X	115035179	115035180	T	C	20	GENIC	homozygous	45198369
X	115033569	115033570	C	T	18	GENIC	possibly homozygous	45198366
X	115033610	115033611	A	G	12	GENIC	possibly homozygous	45198367
X	115033941	115033942	C	T	25	GENIC	possibly homozygous	45198368
X	115035511	115035512	C	T	7	GENIC	homozygous	45198370
X	115035767	115035768	C	T	4	GENIC	homozygous	45198371
X	115037371	115037372	A	AAG	9	GENIC	homozygous	45198375
X	115042248	115042249	T	C	9	GENIC	homozygous	45198377
X	115043250	115043251	A	G	26	GENIC	possibly homozygous	45198378
X	115043322	115043323	A	G	19	GENIC	homozygous	45198379
X	115045109	115045110	G	A	20	GENIC	possibly homozygous	45198380
X	115047086	115047087	C	T	11	GENIC	heterozygous	45198382
X	115047146	115047147	A	G	1	GENIC	homozygous	45198383
X	115049642	115049643	A	C	7	GENIC	homozygous	45198384
X	115051445	115051446	C	T	17	GENIC	possibly homozygous	45198385
X	115051499	115051500	G	A	24	GENIC	homozygous	45198386
X	115053625	115053626	G	A	20	GENIC	possibly homozygous	45198387
X	115053712	115053713	T	C	16	GENIC	homozygous	45198388
X	115054401	115054402	T	TC	12	GENIC	possibly homozygous	45198389
X	115055253	115055254	G	A	17	GENIC	homozygous	45198390