chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40537998	40537999	C	T	54	GENIC	homozygous	115328362
12	40538666	40538667	C	T	44	GENIC	homozygous	115328364
12	40539761	40539762	G	A	50	GENIC	homozygous	115328366
12	40540129	40540130	G	T	44	GENIC	homozygous	115328368
12	40541900	40541901	G	T	34	GENIC	homozygous	115328370
12	40543364	40543365	T	A	58	GENIC	homozygous	115328372
12	40545202	40545203	C	T	38	GENIC	homozygous	115328374
12	40545597	40545598	G	A	10	GENIC	homozygous	115328376
12	40548054	40548055	A	G	20	GENIC	homozygous	115328378
12	40548227	40548228	G	T	37	GENIC	homozygous	115328380
12	40548229	40548230	G	A	37	GENIC	homozygous	115328382
12	40548233	40548234	G	A	38	GENIC	homozygous	115328384
12	40561037	40561038	T	C	22	GENIC	homozygous	115328386
12	40562255	40562256	T	C	56	GENIC	homozygous	115328388
12	40564251	40564252	G	A	46	GENIC	homozygous	115328390
12	40564519	40564520	T	C	43	GENIC	homozygous	115328392
12	40578828	40578829	A	G	49	GENIC	homozygous	115328394
12	40585389	40585390	C	T	31	GENIC	homozygous	115328404
12	40580604	40580605	A	G	34	GENIC	homozygous	115328396
12	40582670	40582671	G	A	41	GENIC	homozygous	115328398
12	40582887	40582888	A	G	37	GENIC	homozygous	115328400
12	40582898	40582899	T	C	41	GENIC	homozygous	115328402
12	40586787	40586788	G	A	66	GENIC	homozygous	115328406
12	40590884	40590885	G	A	33	GENIC	homozygous	115328408
12	40605481	40605482	C	G	29	GENIC	homozygous	115328410
12	40607207	40607208	T	C	30	GENIC	homozygous	115328412
12	40608992	40608993	T	A	40	GENIC	homozygous	115328414
12	40608997	40608998	T	C	36	GENIC	homozygous	115328416
12	40617592	40617593	C	T	33	GENIC	homozygous	115328418