chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	15265666	15265667	T	-	8	GENIC	homozygous	51624349
10	15266178	15266179	T	G	11	GENIC	homozygous	51812207
10	15266228	15266229	A	G	5	GENIC	heterozygous	51812209
10	15266286	15266287	C	T	3	GENIC	homozygous	51812211
10	15266339	15266342	AGG	---	9	GENIC	heterozygous	51812213
10	15266367	15266368	A	AAG	10	GENIC	heterozygous	51812215
10	15266471	15266472	C	A	13	GENIC	homozygous	51812217
10	15266546	15266547	C	T	4	GENIC	heterozygous	51812219
10	15267696	15267697	T	-	3	GENIC	homozygous	51624356
10	15268315	15268316	C	T	18	GENIC	homozygous	51812223
10	15268465	15268466	C	T	13	GENIC	possibly homozygous	51812225
10	15268515	15268516	A	G	14	GENIC	possibly homozygous	51624357
10	15268669	15268670	A	-	11	GENIC	homozygous	51812227
10	15268729	15268730	T	C	4	GENIC	heterozygous	51812229
10	15269229	15269230	G	A	16	GENIC	possibly homozygous	51812233
10	15269498	15269499	A	AT	3	GENIC	homozygous	51812235
10	15269507	15269508	A	T	5	GENIC	heterozygous	52992528
10	15269859	15269860	A	AG	9	GENIC	heterozygous	51812237
10	15269892	15269893	T	C	8	GENIC	homozygous	51812239
10	15270055	15270056	A	G	21	GENIC	possibly homozygous	51812241
10	15270153	15270154	G	A	14	GENIC	homozygous	51812243
10	15270524	15270525	T	-	10	GENIC	homozygous	51812245
10	15271362	15271363	G	A	22	GENIC	heterozygous	51812247
10	15272262	15272263	G	T	24	GENIC	homozygous	51812249
10	15273442	15273443	G	A	13	GENIC	possibly homozygous	51812253
10	15273847	15273849	TG	--	6	GENIC	homozygous	51812255