chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	76321589	76321590	T	G	22	GENIC	homozygous	116801322
10	76322005	76322006	C	T	31	GENIC	homozygous	116801324
10	76322181	76322182	T	C	32	GENIC	homozygous	116801326
10	76323794	76323795	A	G	26	GENIC	homozygous	116801328
10	76323858	76323859	T	G	29	GENIC	homozygous	116801330
10	76323936	76323937	T	C	32	GENIC	homozygous	116801332
10	76327739	76327740	G	T	20	GENIC	homozygous	116894700
10	76328803	76328804	A	T	15	GENIC	homozygous	116801334
10	76329376	76329377	C	T	17	GENIC	homozygous	116801336
10	76329759	76329760	T	C	11	GENIC	homozygous	116801340
10	76331409	76331410	T	G	33	GENIC	homozygous	116801344
10	76331465	76331466	C	T	31	GENIC	homozygous	116801346
10	76331468	76331469	C	T	30	GENIC	homozygous	116801348
10	76331750	76331751	A	G	32	GENIC	homozygous	116801350
10	76331985	76331986	A	G	19	GENIC	homozygous	116801352
10	76333491	76333492	G	A	15	GENIC	homozygous	116801354
10	76333909	76333910	T	C	14	GENIC	homozygous	116942825
10	76334617	76334618	T	C	21	GENIC	homozygous	116801356
10	76334914	76334915	G	A	27	GENIC	homozygous	116801358
10	76335154	76335155	C	T	31	GENIC	homozygous	116801360
10	76335160	76335161	T	C	31	GENIC	homozygous	116801362
10	76335811	76335812	T	C	22	GENIC	homozygous	116801364