chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	41003915	41003916	A	C	74	GENIC	heterozygous	65953482
13	41012866	41012867	C	T	69	GENIC	heterozygous	65953485
13	41012896	41012897	C	T	75	GENIC	heterozygous	65953488
13	41012901	41012902	G	C	74	GENIC	heterozygous	65953491
13	41017162	41017163	T	C	55	GENIC	possibly homozygous	66248919
13	41017722	41017723	C	T	59	GENIC	homozygous	66248921
13	41018120	41018121	G	C	45	GENIC	heterozygous	66248927
13	41018128	41018129	G	C	46	GENIC	heterozygous	66248929
13	41019048	41019049	T	C	55	GENIC	homozygous	66248979
13	41019301	41019302	A	G	59	GENIC	homozygous	66248989
13	41019677	41019678	A	G	58	GENIC	homozygous	66249021
13	41020979	41020980	T	C	47	GENIC	homozygous	66421276
13	41021384	41021385	A	T	25	GENIC	homozygous	66421277
13	41024165	41024166	C	T	65	GENIC	homozygous	66421278
13	41024722	41024723	G	A	12	GENIC	homozygous	66249131
13	41025167	41025168	A	G	58	GENIC	homozygous	66249141
13	41025203	41025204	A	G	61	GENIC	homozygous	66249143
13	41025581	41025582	C	G	43	GENIC	homozygous	66249145
13	41025707	41025708	G	A	44	GENIC	possibly homozygous	66421279
13	41025749	41025750	A	G	44	GENIC	homozygous	66249147
13	41026046	41026047	C	A	27	GENIC	heterozygous	65953493
13	41026240	41026241	G	A	15	GENIC	homozygous	66249151
13	41026242	41026243	G	A	13	GENIC	homozygous	66249153
13	41026331	41026332	G	T	28	GENIC	possibly homozygous	65953496
13	41026370	41026371	C	G	33	GENIC	homozygous	65953499
13	41026382	41026383	C	A	37	GENIC	possibly homozygous	65953502
13	41039033	41039034	A	C	36	GENIC	homozygous	66421281
13	41041166	41041167	A	T	37	GENIC	homozygous	66249177
13	41041453	41041454	C	T	44	GENIC	homozygous	66421282
13	41042498	41042499	A	T	65	GENIC	homozygous	66421283
13	41042524	41042525	A	G	77	GENIC	homozygous	66249185
13	41042390	41042391	G	T	31	GENIC	heterozygous	66463026