chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	40438497	40438498	T	A	5	GENIC	homozygous	116569252
10	40439908	40439909	T	C	29	GENIC	homozygous	116569254
10	40441111	40441112	G	A	28	GENIC	homozygous	116569256
10	40441458	40441459	C	T	21	GENIC	possibly homozygous	116569258
10	40441660	40441661	C	T	23	GENIC	homozygous	116569260
10	40443489	40443490	T	C	31	GENIC	homozygous	116569262
10	40444932	40444933	T	G	22	GENIC	homozygous	116569264
10	40445431	40445432	A	G	31	GENIC	homozygous	116569266
10	40445575	40445576	G	A	31	GENIC	possibly homozygous	116569268
10	40445784	40445785	A	T	35	GENIC	homozygous	116569270
10	40446639	40446640	C	T	18	GENIC	homozygous	116569272
10	40447474	40447475	A	G	20	GENIC	homozygous	116569278
10	40449612	40449613	T	C	15	GENIC	homozygous	116569280
10	40449639	40449640	G	C	16	GENIC	homozygous	116569282
10	40449961	40449962	A	C	11	GENIC	homozygous	116569284
10	40450189	40450190	G	A	12	GENIC	homozygous	116569286
10	40450385	40450386	A	G	10	GENIC	homozygous	116569288
10	40450626	40450627	C	A	9	GENIC	possibly homozygous	116569290
10	40450648	40450649	A	G	7	GENIC	homozygous	116569292
10	40450399	40450400	T	C	13	GENIC	homozygous	117005481
10	40448995	40448996	C	T	18	GENIC	homozygous	117005479