chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	1288119	1288120	A	G	22	GENIC	homozygous	108215850
X	1288793	1288794	C	T	24	GENIC	homozygous	108215853
X	1289085	1289086	A	G	19	GENIC	homozygous	108215855
X	1289515	1289516	G	A	20	GENIC	homozygous	108215858
X	1291207	1291208	G	A	26	GENIC	homozygous	108215860
X	1292805	1292806	A	G	17	GENIC	homozygous	108215862
X	1293302	1293303	G	A	18	GENIC	homozygous	108215865
X	1298595	1298596	A	G	25	GENIC	homozygous	108215867
X	1300964	1300965	A	G	20	GENIC	homozygous	108215870
X	1304396	1304397	G	A	18	GENIC	homozygous	108215873
X	1299216	1299217	A		22	GENIC	homozygous	129715145
X	1294676	1294683	AGACTCT		34	GENIC	homozygous	129715143
X	1304507	1304507		C	30	GENIC	homozygous	129715146