chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	45041846	45041847	G	T	38	GENIC	homozygous	115853388
11	45041847	45041848	T	G	38	GENIC	homozygous	115853390
11	45041902	45041903	C	A	41	GENIC	homozygous	115853392
11	45041903	45041904	A	C	40	GENIC	homozygous	115853394
11	45042151	45042152	T	G	22	GENIC	homozygous	115853396
11	45042152	45042153	C	T	22	GENIC	homozygous	115853398
11	45042195	45042196	T	G	34	GENIC	homozygous	115963427
11	45042196	45042197	C	T	34	GENIC	homozygous	115963428
11	45076523	45076524	C	G	23	GENIC	homozygous	115853466
11	45222066	45222067	A	G	28	GENIC	homozygous	115853681