chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	26972237	26972238	G	A	14	GENIC	homozygous	114303262
13	26973744	26973745	T	C	25	GENIC	homozygous	114303263
13	26974230	26974231	C	G	27	GENIC	homozygous	114303264
13	26974232	26974233	C	G	28	GENIC	homozygous	114303265
13	26974461	26974462	T	C	21	GENIC	homozygous	114303266
13	26975837	26975838	A	G	14	GENIC	homozygous	114303267
13	26977115	26977116	G	A	9	GENIC	homozygous	114303268
13	26978944	26978945	T	G	17	GENIC	homozygous	114303269
13	26979655	26979656	C	T	20	GENIC	homozygous	114303270
13	26981199	26981200	T	C	20	GENIC	homozygous	114516659
13	26994024	26994025	T	C	23	GENIC	homozygous	114303271
13	26994083	26994084	T	C	28	GENIC	homozygous	114303272
13	26994158	26994159	G	A	26	GENIC	homozygous	114303273
13	26994385	26994386	C	T	15	GENIC	heterozygous	114662188
13	26994909	26994910	C	T	25	GENIC	possibly homozygous	114303274
13	26994940	26994941	T	C	23	GENIC	homozygous	114303275
13	26995118	26995119	A	G	27	GENIC	homozygous	114303276
13	26995873	26995874	T	C	22	GENIC	possibly homozygous	114303277
13	26996337	26996338	G	T	21	GENIC	homozygous	114303278
13	26997331	26997332	G	A	11	GENIC	homozygous	114303279
13	26997336	26997337	A	T	11	GENIC	homozygous	114303280
13	26997344	26997345	C	A	14	GENIC	homozygous	114303281
13	26997362	26997363	T	C	15	GENIC	homozygous	114303282
13	26997706	26997707	T	C	25	GENIC	homozygous	114303283
13	26997752	26997753	T	C	21	GENIC	homozygous	114303284
13	26998157	26998158	T	C	33	GENIC	homozygous	114303285
13	26998180	26998181	T	C	31	GENIC	homozygous	114303286
13	26998949	26998950	G	A	39	GENIC	homozygous	114303287
13	26999447	26999448	G	A	24	GENIC	homozygous	114303288
13	26999563	26999564	C	T	20	GENIC	homozygous	114303289
13	26994379	26994380	T	C	16	GENIC	heterozygous	114944486
13	26996251	26996252	A	G	16	GENIC	homozygous	114608643