chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	35155869	35155870	G	T	20	GENIC	homozygous	115822281
11	35155870	35155871	T	G	20	GENIC	homozygous	115822283
11	35192187	35192188	G	A	6	GENIC	homozygous	115822450
11	35200527	35200528	C	G	26	GENIC	homozygous	115822488
11	35200577	35200578	A	G	24	GENIC	homozygous	115822490
11	35200771	35200772	A	G	23	GENIC	homozygous	115822494
11	35200918	35200919	A	G	13	GENIC	homozygous	115961775
11	35206201	35206202	A	C	26	GENIC	homozygous	115822506
11	35206709	35206710	G	T	19	GENIC	homozygous	115961776
11	35206710	35206711	T	C	19	GENIC	homozygous	115961777
11	35208757	35208758	A	C	28	GENIC	homozygous	115961779
11	35208758	35208759	G	A	25	GENIC	homozygous	115822514
11	35227712	35227713	T	G	14	GENIC	homozygous	115822585
11	35228348	35228349	T	G	16	GENIC	homozygous	116109703
11	35228349	35228350	G	T	15	GENIC	homozygous	116109704
11	35257933	35257934	T	C	2	GENIC	homozygous	115961791
11	35257963	35257964	T	A	2	GENIC	homozygous	115961792
11	35257965	35257966	C	T	2	GENIC	homozygous	115961793