chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	24402946	24402947	A	C	66	GENIC	possibly homozygous	119039602
5	24403793	24403793		TG	32	GENIC	possibly homozygous	130951401
5	24405259	24405259		G	15	GENIC	possibly homozygous	130951402
5	24406011	24406011		A	63	GENIC	homozygous	130951403
5	24412307	24412307		CAAA	62	GENIC	homozygous	130951404
5	24412583	24412584	G	C	63	GENIC	homozygous	118970443
5	24404309	24404310	A	T	63	GENIC	homozygous	118970439
5	24410387	24410388	C	T	69	GENIC	homozygous	118970441
5	24406770	24406771	G	C	44	GENIC	homozygous	113689982
5	24406284	24406285	A	T	43	GENIC	possibly homozygous	119008858
5	24405416	24405488	TCAGACATAAAATAAGTAAATCTGGAAGGAAGGAAGGAGGAAGGAAGGAAGGAAGGAAAGAAAGAAAGAAAG		14	GENIC	homozygous	129913047
5	24413265	24413328	GGTCCCCAGCTCCAAAAAAAAAAAAAAAAAAAAAAAAAGAGCGTGGCTGCTGCTCTTTCATTT		51	GENIC	homozygous	130951405
5	24414840	24414841	A	G	69	GENIC	homozygous	118970445
5	24415074	24415075	G	A	35	GENIC	homozygous	119008859
5	24415131	24415132	T		45	GENIC	homozygous	130951406
5	24417171	24417172	C	T	46	GENIC	homozygous	118970447
5	24417299	24417299		CCA	9	GENIC	homozygous	130951407
5	24418745	24418746	T	C	67	GENIC	homozygous	118970449