chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	40438497	40438498	T	A	14	GENIC	homozygous	116569252
10	40439908	40439909	T	C	13	GENIC	homozygous	116569254
10	40441111	40441112	G	A	26	GENIC	homozygous	116569256
10	40441458	40441459	C	T	34	GENIC	homozygous	116569258
10	40441660	40441661	C	T	20	GENIC	homozygous	116569260
10	40443489	40443490	T	C	22	GENIC	homozygous	116569262
10	40444932	40444933	T	G	19	GENIC	homozygous	116569264
10	40445431	40445432	A	G	30	GENIC	homozygous	116569266
10	40445575	40445576	G	A	15	GENIC	homozygous	116569268
10	40445784	40445785	A	T	29	GENIC	homozygous	116569270
10	40446639	40446640	C	T	26	GENIC	homozygous	116569272
10	40446932	40446933	C	T	13	GENIC	homozygous	116569274
10	40447460	40447461	G	A	20	GENIC	homozygous	116569276
10	40447474	40447475	A	G	24	GENIC	homozygous	116569278
10	40449612	40449613	T	C	15	GENIC	homozygous	116569280
10	40449639	40449640	G	C	17	GENIC	homozygous	116569282
10	40449961	40449962	A	C	18	GENIC	homozygous	116569284
10	40450189	40450190	G	A	16	GENIC	homozygous	116569286
10	40450385	40450386	A	G	13	GENIC	homozygous	116569288
10	40450626	40450627	C	A	8	GENIC	homozygous	116569290
10	40450648	40450649	A	G	7	GENIC	homozygous	116569292