chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	120624951	120624952	G	C	23	GENIC	homozygous	108811466
X	120625906	120625907	G	T	37	GENIC	homozygous	108421287
X	120626025	120626026	A	C	34	GENIC	homozygous	108421290
X	120627353	120627354	C	G	18	GENIC	homozygous	108421294
X	120631584	120631585	A	G	29	GENIC	homozygous	108811468
X	120632615	120632616	A	G	26	GENIC	homozygous	108421314
X	120633059	120633060	A	G	32	GENIC	homozygous	108421316
X	120634237	120634238	C	A	23	GENIC	homozygous	108421320
X	120637018	120637019	G	C	35	GENIC	homozygous	108421330
X	120637500	120637501	C	T	36	GENIC	homozygous	108811470
X	120638623	120638624	T	C	27	GENIC	homozygous	108421338
X	120639577	120639578	C	G	26	GENIC	homozygous	108811472
X	120640164	120640165	C	A	33	GENIC	homozygous	108811474
X	120641965	120641966	C	T	30	GENIC	homozygous	108811476
X	120643596	120643597	G	A	28	GENIC	homozygous	108811478
X	120643672	120643672		TATA	31	GENIC	homozygous	135245307
X	120634197	120634198	A		23	GENIC	homozygous	135245304
X	120635487	120635487		ATATATATATATATATA	7	GENIC	heterozygous	135245305
X	120642337	120642345	ATATATAC		19	GENIC	homozygous	135245306
X	120639633	120639633		AAG	30	GENIC	homozygous	131243523
X	120641993	120641994	C	T	28	GENIC	homozygous	108818622
X	120643844	120643845	T		23	GENIC	homozygous	135245308
X	120643946	120643947	A	G	26	GENIC	homozygous	108811480
X	120644114	120644115	T	G	27	GENIC	possibly homozygous	108818623
X	120646064	120646065	G	A	28	GENIC	homozygous	108811482
X	120647125	120647129	ATTA		32	GENIC	homozygous	135245309
X	120647289	120647290	A	G	21	GENIC	homozygous	108811484
X	120647545	120647546	T	G	31	GENIC	homozygous	108811486
X	120647666	120647667	G	A	26	GENIC	homozygous	108811488