chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	74035294	74035295	A	G	17	GENIC	homozygous	114391216
13	74035365	74035366	T	C	11	GENIC	homozygous	114391218
13	74036739	74036740	G	A	16	GENIC	homozygous	114391220
13	74037350	74037351	G	A	18	GENIC	homozygous	114391222
13	74039367	74039368	G	A	25	GENIC	homozygous	114391224
13	74041119	74041120	T	C	8	GENIC	heterozygous	118461884
13	74045987	74045988	A	G	21	GENIC	homozygous	114391228
13	74048476	74048477	C	A	17	GENIC	homozygous	114391230
13	74048742	74048743	C	A	21	GENIC	homozygous	114391232
13	74048869	74048870	C	T	14	GENIC	homozygous	114640183
13	74049072	74049073	T	C	29	GENIC	homozygous	114391234
13	74050199	74050200	G	A	20	GENIC	homozygous	114391236
13	74050249	74050250	G	A	7	GENIC	homozygous	126068688
13	74043041	74043042	C	T	19	GENIC	homozygous	126068686
13	74050230	74050231	G	C	12	GENIC	homozygous	126068687
13	74050260	74050261	C	T	7	GENIC	homozygous	126068689
13	74050825	74050826	G	A	13	GENIC	homozygous	114391238
13	74053276	74053277	G	A	27	GENIC	homozygous	114391240
13	74056157	74056158	A	T	13	GENIC	homozygous	114391242
13	74057099	74057100	T	C	14	GENIC	homozygous	114391244
13	74057369	74057370	C	T	17	GENIC	homozygous	114391246
13	74060951	74060952	G	A	11	GENIC	homozygous	114391248
13	74061407	74061408	G	C	14	GENIC	heterozygous	118461885
13	74062551	74062552	G	T	14	GENIC	homozygous	114391250
13	74062732	74062733	A	G	22	GENIC	homozygous	114391252
13	74063728	74063729	G	A	19	GENIC	homozygous	114391254
13	74065238	74065239	T	C	20	GENIC	homozygous	114391256
13	74065736	74065737	T	G	24	GENIC	homozygous	114391258
13	74069671	74069672	C	T	21	GENIC	homozygous	118461889
13	74071244	74071245	A	T	24	GENIC	homozygous	114391260
13	74074208	74074209	T	C	29	GENIC	homozygous	114391262