chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	25734782	25734783	C	T	9	GENIC	homozygous	113696978
5	25736129	25736130	T	A	14	GENIC	homozygous	113696980
5	25738710	25738711	A	T	9	GENIC	homozygous	113696982
5	25741147	25741148	A	G	17	GENIC	homozygous	113696984
5	25741222	25741223	G	C	14	GENIC	heterozygous	113696986
5	25742247	25742248	C	T	16	GENIC	homozygous	113696994
5	25743337	25743338	T	C	8	GENIC	homozygous	113696996
5	25744230	25744231	A	G	25	GENIC	homozygous	113696998
5	25744299	25744300	C	T	15	GENIC	homozygous	113697000
5	25744532	25744533	A	G	15	GENIC	homozygous	113697002
5	25744780	25744781	T	C	15	GENIC	homozygous	113697004
5	25745580	25745581	A	G	16	GENIC	homozygous	113697006
5	25747014	25747015	C	T	11	GENIC	heterozygous	113697008
5	25747395	25747396	T	C	20	GENIC	homozygous	113697010
5	25748421	25748422	T	G	16	GENIC	homozygous	113697012
5	25748554	25748555	A	G	15	GENIC	homozygous	113697014
5	25749067	25749068	A	G	21	GENIC	homozygous	113697018
5	25749131	25749132	G	A	14	GENIC	homozygous	113697020
5	25750933	25750934	T	C	15	GENIC	homozygous	113697022