chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	41974051	41974052	C	T	16	GENIC	homozygous	113437746
14	41974052	41974053	A	C	17	GENIC	homozygous	113437748
14	41992580	41992581	G	T	11	GENIC	homozygous	113437760
14	41992626	41992627	A	T	8	GENIC	homozygous	113437762
14	41992627	41992628	G	A	7	GENIC	homozygous	113437764
14	41992514	41992515	T	A	11	GENIC	homozygous	113591573
14	41992515	41992516	A	T	11	GENIC	homozygous	113591575
14	42041618	42041619	C	G	22	GENIC	homozygous	113437947
14	42066649	42066650	G	A	16	GENIC	homozygous	113591581
14	42071261	42071262	A	T	2	GENIC	homozygous	113676190
14	42077760	42077761	G	T	29	GENIC	possibly homozygous	113438089
14	42078174	42078175	T	C	14	GENIC	homozygous	113438091
14	42099324	42099325	A	T	8	GENIC	homozygous	113438118
14	42122560	42122561	T	A	38	GENIC	homozygous	113438282
14	42159017	42159018	G	T	13	GENIC	homozygous	113438445
14	42164149	42164150	A	T	33	GENIC	homozygous	113438455
14	42202783	42202784	T	A	26	GENIC	homozygous	113591598
14	42124491	42124492	A	G	14	GENIC	homozygous	113867308