chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	41917149	41917150	T	G	34	GENIC	homozygous	114772390
6	41918159	41918160	A	G	29	GENIC	homozygous	114772394
6	41918173	41918174	T	C	30	GENIC	homozygous	114772396
6	41918255	41918256	G	C	19	GENIC	homozygous	114772398
6	41918649	41918650	G	A	32	GENIC	homozygous	114772408
6	41919525	41919526	T	A	26	GENIC	homozygous	115206448
6	41919981	41919982	T	C	23	GENIC	possibly homozygous	115206449
6	41920404	41920405	C	T	26	GENIC	homozygous	115206450
6	41920507	41920508	T	C	29	GENIC	homozygous	115206451
6	41920688	41920689	T	C	22	GENIC	homozygous	115206452
6	41920697	41920698	C	T	23	GENIC	homozygous	115206453
6	41920799	41920800	A	G	24	GENIC	homozygous	115206454
6	41920875	41920876	A	G	30	GENIC	homozygous	115206455
6	41920896	41920897	C	T	35	GENIC	homozygous	115206456
6	41921025	41921026	G	A	35	GENIC	homozygous	115206457
6	41921162	41921163	C	G	32	GENIC	possibly homozygous	114772414
6	41921192	41921193	C	G	33	GENIC	homozygous	115206458
6	41921538	41921539	T	C	35	GENIC	homozygous	115206459
6	41922243	41922244	G	A	25	GENIC	homozygous	115206460
6	41922246	41922247	A	G	28	GENIC	homozygous	115206461
6	41923481	41923482	C	T	34	GENIC	homozygous	115206462