chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	76742343	76742344	C	T	28	GENIC	homozygous	116200686
11	76742932	76742933	A	G	29	GENIC	homozygous	116057480
11	76743275	76743276	T	C	29	GENIC	homozygous	116200695
11	76743587	76743588	A	G	29	GENIC	homozygous	116057482
11	76743672	76743673	T	C	37	GENIC	homozygous	116057484
11	76744386	76744387	G	T	46	GENIC	homozygous	116280675
11	76744525	76744526	T	C	36	GENIC	homozygous	116057490
11	76744754	76744755	C	T	27	GENIC	homozygous	116057496
11	76748584	76748585	G	A	27	GENIC	homozygous	116356724
11	76744499	76744500	C	G	33	GENIC	homozygous	116356721
11	76744549	76744550	T	A	39	GENIC	homozygous	116356722
11	76745674	76745675	G	A	22	GENIC	homozygous	116356723
11	76751240	76751241	A	G	17	GENIC	homozygous	116057524
11	76751285	76751286	A	G	23	GENIC	homozygous	116057526
11	76768645	76768646	G	A	21	GENIC	homozygous	116356725
11	76780914	76780915	A	G	27	GENIC	homozygous	116057666
11	76784404	76784405	C	T	23	GENIC	homozygous	116057692
11	76784597	76784598	G	A	22	GENIC	homozygous	116356726
11	76786236	76786237	A	G	18	GENIC	homozygous	116356727
11	76791263	76791264	A	G	34	GENIC	homozygous	116057708
11	76792934	76792935	T	C	31	GENIC	homozygous	116057710
11	76794841	76794842	A	G	21	GENIC	homozygous	116057725
11	76795097	76795098	G	T	25	GENIC	homozygous	116057733
11	76803878	76803879	C	T	22	GENIC	homozygous	116200825
11	76803950	76803951	G	T	24	GENIC	homozygous	116356729
11	76803953	76803954	A	G	26	GENIC	homozygous	116356730