chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	10722219	10722220	G	A	57	GENIC	homozygous	111724159
16	10722244	10722245	C	T	61	GENIC	homozygous	111724161
16	10722317	10722318	G	A	56	GENIC	possibly homozygous	111724163
16	10722518	10722519	A	G	61	GENIC	homozygous	111724165
16	10722629	10722630	C	T	45	GENIC	homozygous	111724167
16	10722901	10722902	G	A	42	GENIC	homozygous	111724169
16	10722947	10722948	G	A	45	GENIC	homozygous	111724171
16	10723045	10723046	A	G	59	GENIC	homozygous	111724173
16	10723046	10723047	T	C	59	GENIC	homozygous	111724175
16	10723120	10723121	C	T	48	GENIC	homozygous	111724178
16	10723605	10723606	G	T	28	GENIC	homozygous	111724180
16	10724283	10724284	T	C	47	GENIC	homozygous	111724182
16	10724389	10724390	T	C	56	GENIC	homozygous	111724184
16	10724627	10724628	A	G	32	GENIC	homozygous	119095071
16	10724972	10724973	C	T	42	GENIC	possibly homozygous	119095072
16	10725105	10725106	C	T	52	GENIC	homozygous	111724186
16	10725273	10725274	G	C	55	GENIC	homozygous	111724188
16	10725582	10725583	C	G	38	GENIC	homozygous	111724190
16	10725760	10725761	G	A	57	GENIC	homozygous	111724192
16	10725797	10725798	A	G	48	GENIC	homozygous	111724194
16	10726145	10726146	A	G	41	GENIC	homozygous	111724196
16	10726359	10726360	T	C	41	GENIC	homozygous	111724198