chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	73693874	73693875	G	A	32	GENIC	homozygous	115990022
11	73694406	73694407	A	G	15	GENIC	homozygous	116054163
11	73694569	73694570	T	C	23	GENIC	homozygous	115990024
11	73696045	73696046	T	A	17	GENIC	homozygous	115990026
11	73696368	73696369	G	A	33	GENIC	homozygous	115990028
11	73696751	73696752	A	G	38	GENIC	homozygous	115990030
11	73707317	73707318	G	A	13	GENIC	homozygous	115990032
11	73707318	73707319	A	T	13	GENIC	homozygous	115990034
11	73707465	73707466	A	C	23	GENIC	homozygous	115990036
11	73707901	73707902	G	A	28	GENIC	homozygous	115990038
11	73708254	73708255	C	T	22	GENIC	homozygous	115990040
11	73710775	73710776	C	T	36	GENIC	homozygous	115990044
11	73711131	73711132	G	A	19	GENIC	homozygous	115990046
11	73712010	73712011	C	T	15	GENIC	homozygous	115990048
11	73712709	73712710	G	A	25	GENIC	homozygous	116054169
11	73713783	73713784	T	C	32	GENIC	homozygous	115990050
11	73714592	73714593	A	G	24	GENIC	homozygous	115990052
11	73715065	73715066	G	A	19	GENIC	homozygous	116248152
11	73715145	73715146	A	C	26	GENIC	homozygous	115990054
11	73718653	73718654	C	A	11	GENIC	homozygous	116248154
11	73718697	73718698	G	A	11	GENIC	homozygous	115990056
11	73719091	73719092	C	T	28	GENIC	homozygous	115990058
11	73719218	73719219	G	A	25	GENIC	homozygous	115990060
11	73719602	73719603	T	C	27	GENIC	homozygous	115990062
11	73721805	73721806	A	T	35	GENIC	homozygous	115990064