chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	45041846	45041847	G	T	28	GENIC	homozygous	115853388
11	45041847	45041848	T	G	28	GENIC	homozygous	115853390
11	45041902	45041903	C	A	21	GENIC	homozygous	115853392
11	45041903	45041904	A	C	21	GENIC	homozygous	115853394
11	45042151	45042152	T	G	20	GENIC	homozygous	115853396
11	45042152	45042153	C	T	20	GENIC	homozygous	115853398
11	45042195	45042196	T	G	24	GENIC	homozygous	115963427
11	45042196	45042197	C	T	23	GENIC	homozygous	115963428
11	45047038	45047039	G	T	28	GENIC	homozygous	115853412
11	45047043	45047044	T	C	30	GENIC	homozygous	115853414
11	45047059	45047060	G	T	28	GENIC	homozygous	115853416
11	45047065	45047066	G	C	27	GENIC	homozygous	115853418
11	45076523	45076524	C	G	23	GENIC	homozygous	115853466
11	45217592	45217593	T	G	16	GENIC	possibly homozygous	115963431
11	45222066	45222067	A	G	18	GENIC	homozygous	115853681