chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	41017162	41017163	T	C	16	GENIC	homozygous	66248919
13	41017722	41017723	C	T	26	GENIC	homozygous	66248921
13	41019048	41019049	T	C	15	GENIC	homozygous	66248979
13	41019301	41019302	A	G	20	GENIC	homozygous	66248989
13	41019677	41019678	A	G	19	GENIC	homozygous	66249021
13	41020979	41020980	T	C	23	GENIC	homozygous	66421276
13	41021384	41021385	A	T	11	GENIC	homozygous	66421277
13	41024165	41024166	C	T	24	GENIC	homozygous	66421278
13	41024722	41024723	G	A	6	GENIC	homozygous	66249131
13	41025167	41025168	A	G	16	GENIC	homozygous	66249141
13	41025203	41025204	A	G	11	GENIC	homozygous	66249143
13	41025581	41025582	C	G	10	GENIC	homozygous	66249145
13	41025707	41025708	G	A	24	GENIC	possibly homozygous	66421279
13	41025749	41025750	A	G	17	GENIC	homozygous	66249147
13	41026240	41026241	G	A	9	GENIC	homozygous	66249151
13	41026242	41026243	G	A	9	GENIC	homozygous	66249153
13	41039033	41039034	A	C	6	GENIC	homozygous	66421281
13	41041166	41041167	A	T	14	GENIC	possibly homozygous	66249177
13	41041453	41041454	C	T	22	GENIC	homozygous	66421282
13	41042498	41042499	A	T	18	GENIC	homozygous	66421283
13	41042524	41042525	A	G	16	GENIC	homozygous	66249185