chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	26972237	26972238	G	A	18	GENIC	homozygous	114303262
13	26973744	26973745	T	C	16	GENIC	homozygous	114303263
13	26974230	26974231	C	G	15	GENIC	homozygous	114303264
13	26974232	26974233	C	G	15	GENIC	homozygous	114303265
13	26974461	26974462	T	C	13	GENIC	homozygous	114303266
13	26975837	26975838	A	G	14	GENIC	homozygous	114303267
13	26976637	26976638	A	G	33	GENIC	homozygous	114745264
13	26977115	26977116	G	A	22	GENIC	homozygous	114303268
13	26979655	26979656	C	T	8	GENIC	homozygous	114303270
13	26980474	26980475	A	T	29	GENIC	homozygous	114516657
13	26981199	26981200	T	C	27	GENIC	homozygous	114516659
13	26994024	26994025	T	C	8	GENIC	homozygous	114303271
13	26994083	26994084	T	C	10	GENIC	homozygous	114303272
13	26994158	26994159	G	A	4	GENIC	homozygous	114303273
13	26994909	26994910	C	T	18	GENIC	homozygous	114303274
13	26994940	26994941	T	C	20	GENIC	homozygous	114303275
13	26995118	26995119	A	G	12	GENIC	homozygous	114303276
13	26995873	26995874	T	C	13	GENIC	possibly homozygous	114303277
13	26996251	26996252	A	G	13	GENIC	homozygous	114608643
13	26996337	26996338	G	T	23	GENIC	homozygous	114303278
13	26997362	26997363	T	C	15	GENIC	homozygous	114303282
13	26997706	26997707	T	C	32	GENIC	homozygous	114303283
13	26997752	26997753	T	C	36	GENIC	homozygous	114303284
13	26998157	26998158	T	C	11	GENIC	homozygous	114303285
13	26998180	26998181	T	C	14	GENIC	homozygous	114303286
13	26998949	26998950	G	A	32	GENIC	homozygous	114303287
13	26999447	26999448	G	A	20	GENIC	homozygous	114303288
13	26999563	26999564	C	T	14	GENIC	homozygous	114303289