chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	30912377	30912378	G	A	59	GENIC	homozygous	145764846
11	30912484	30912485	T	C	52	GENIC	homozygous	138953082
11	30912803	30912804	T		52	GENIC	homozygous	145753285
11	30913777	30913778	A		66	GENIC	homozygous	138880826
11	30914683	30914684	A	C	42	GENIC	homozygous	145764847
11	30919001	30919002	T	C	55	GENIC	homozygous	138953086
11	30919586	30919587	T	C	34	GENIC	homozygous	138953087
11	30920445	30920445		G	46	GENIC	homozygous	145753286
11	30920447	30920448	A	C	46	GENIC	homozygous	145764848
11	30921107	30921108	T	C	55	GENIC	homozygous	138953089
11	30921827	30921828	T	C	47	GENIC	homozygous	145764849
11	30921839	30921840	G	A	47	GENIC	homozygous	138953091
11	30923462	30923463	C	A	49	GENIC	homozygous	145764850
11	30925276	30925277	T	G	49	GENIC	possibly homozygous	138953096
11	30926184	30926185	A	G	56	GENIC	homozygous	145764851
11	30927526	30927527	A	C	39	GENIC	homozygous	138953100
11	30927528	30927529	A	G	40	GENIC	homozygous	138953101
11	30929659	30929659		AC	32	GENIC	homozygous	145753287
11	30930256	30930257	A	G	46	GENIC	homozygous	145764852
11	30933076	30933077	T	C	54	GENIC	homozygous	145764853
11	30926349	30926350	T		12	GENIC	heterozygous	403302838
11	30926349	30926350	T	A	12	GENIC	heterozygous	403302839