chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	22313290	22313291	G	T	26	GENIC	homozygous	108238721
X	22313293	22313294	G	T	26	GENIC	homozygous	108238723
X	22313294	22313295	G	A	26	GENIC	homozygous	108238726
X	22313309	22313310	G	T	29	GENIC	homozygous	108238728
X	22313315	22313316	G		27	GENIC	homozygous	129727098
X	22313318	22313319	G	C	28	GENIC	homozygous	108238730
X	22313318	22313318		T	27	GENIC	homozygous	129727099
X	22313327	22313328	G	A	29	GENIC	homozygous	108238732
X	22313500	22313500		CAGCATGGCACTGGACTAGGTTGCATTAAGTAGAAAAGTAGATCTTGTGGGCCCTGCCTGCAGGCAACTTACTTAATTGGGGAAAACAAAGGCAGCTAATTTGGAACAAAAACCAAAA	24	GENIC	possibly homozygous	129727100
X	22320935	22320936	A	T	30	GENIC	homozygous	108238742
X	22322017	22322019	GG		15	GENIC	homozygous	129727101
X	22322031	22322032	G		12	GENIC	homozygous	129727102
X	22322039	22322040	G		10	GENIC	homozygous	129727103
X	22331660	22331661	G		5	GENIC	homozygous	129727104
X	22332076	22332077	T		10	GENIC	homozygous	129727106
X	22332189	22332190	G		13	GENIC	homozygous	129727107
X	22332230	22332232	AT		16	GENIC	homozygous	129727108
X	22332266	22332266		A	17	GENIC	homozygous	129727109
X	22332284	22332284		TA	18	GENIC	homozygous	129727110
X	22332593	22332593		A	11	GENIC	homozygous	129727111
X	22332599	22332599		A	11	GENIC	homozygous	129727112
X	22340388	22340388		C	29	GENIC	homozygous	129727115
X	22344535	22344535		CAT	20	GENIC	homozygous	129727117
X	22318257	22318262	CTTTA		38	GENIC	heterozygous	130496987
X	22318271	22318272	C	T	39	GENIC	heterozygous	120047487
X	22332518	22332519	G	T	6	GENIC	homozygous	108439679
X	22339822	22339823	G	T	6	GENIC	heterozygous	108439681