chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	274616718	274616719	G	A	44	GENIC	homozygous	108655233
1	274616794	274616795	C	T	39	GENIC	homozygous	108655235
1	274618088	274618089	C	T	56	GENIC	homozygous	108655239
1	274618249	274618250	A	C	45	GENIC	homozygous	108655241
1	274618882	274618884	AC		6	GENIC	heterozygous	133601444
1	274619418	274619419	C	T	12	GENIC	homozygous	108655257
1	274619439	274619439		ACACAGACACACAG	13	GENIC	homozygous	127513008
1	274619564	274619565	G	C	40	GENIC	possibly homozygous	108655262
1	274619570	274619571	C	G	39	GENIC	possibly homozygous	108655264
1	274619663	274619664	G	A	46	GENIC	homozygous	108655266
1	274620081	274620082	A	G	49	GENIC	homozygous	108655268
1	274620217	274620218	G	A	50	GENIC	homozygous	108655270
1	274620235	274620236	C	T	49	GENIC	homozygous	108655271
1	274620550	274620551	T		47	GENIC	homozygous	127513009
1	274620980	274620981	G	A	60	GENIC	homozygous	108655273
1	274621008	274621014	GGCCTC		62	GENIC	homozygous	127513010
1	274621733	274621734	A	C	62	GENIC	homozygous	108655275
1	274621818	274621819	G	A	61	GENIC	homozygous	108655277
1	274641490	274641491	T	C	55	GENIC	homozygous	108655279
1	274641942	274641943	T	C	35	GENIC	homozygous	108655281