chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	62106831	62106832	G	A	27	GENIC	homozygous	116110151
11	62106991	62106992	T	C	38	GENIC	heterozygous	118161896
11	62132120	62132121	T	A	12	GENIC	homozygous	118161897
11	62132612	62132613	T	G	18	GENIC	homozygous	118161898
11	62132716	62132717	T	C	20	GENIC	homozygous	116159379
11	62168195	62168196	G	A	29	GENIC	homozygous	116104957
11	62341267	62341268	T	A	24	GENIC	homozygous	115877736
11	62341354	62341355	A	G	21	GENIC	heterozygous	116417870
11	62280367	62280368	A	G	51	GENIC	heterozygous	118195185
11	62280394	62280395	C	T	66	GENIC	heterozygous	118195186
11	62363354	62363355	C	A	31	GENIC	heterozygous	118195187
11	62378457	62378458	A	C	13	GENIC	homozygous	118195188
11	62384343	62384344	T	A	46	GENIC	heterozygous	118195189
11	62402567	62402568	G	C	77	GENIC	heterozygous	118195190
11	62405697	62405698	T	C	81	GENIC	heterozygous	118195191
11	62405778	62405779	G	A	82	GENIC	heterozygous	118195192
11	62416678	62416679	T	G	29	GENIC	heterozygous	118195193
11	62428152	62428153	C	T	27	GENIC	homozygous	115877738
11	62435901	62435902	G	A	26	GENIC	heterozygous	118195194
11	62545453	62545454	G	A	35	GENIC	heterozygous	116223292
11	62559290	62559291	G	T	8	GENIC	homozygous	118161913