chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	94232093	94232094	G	A	26	GENIC	homozygous	116954777
10	94233989	94233990	C	A	25	GENIC	homozygous	116954779
10	94235886	94235887	A	C	21	GENIC	homozygous	116954781
10	94239606	94239607	G	A	28	GENIC	homozygous	116954783
10	94240523	94240524	G	A	36	GENIC	homozygous	116684949
10	94242190	94242191	A	G	45	GENIC	homozygous	116954785
10	94242234	94242235	G	C	37	GENIC	possibly homozygous	116954787
10	94242472	94242473	C	T	15	GENIC	homozygous	116684957
10	94242503	94242504	C	T	11	GENIC	homozygous	116954789
10	94242777	94242778	A	G	21	GENIC	homozygous	116684959
10	94244313	94244314	T	A	23	GENIC	homozygous	116826180
10	94244921	94244922	C	T	28	GENIC	homozygous	116954791
10	94247657	94247658	C	T	25	GENIC	homozygous	116954793
10	94248793	94248794	G	A	29	GENIC	homozygous	116954795
10	94249288	94249289	C	T	31	GENIC	homozygous	116826182
10	94250698	94250699	T	C	28	GENIC	homozygous	116684982
10	94251102	94251103	T	C	36	GENIC	homozygous	116684984
10	94251208	94251209	A	G	32	GENIC	homozygous	116684986
10	94253382	94253383	C	T	33	GENIC	homozygous	116954797