chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	49306455	49306456	A	G	38	GENIC	homozygous	116882358
10	49306857	49306858	T	C	27	GENIC	homozygous	116932011
10	49306875	49306876	G	A	30	GENIC	homozygous	116932013
10	49307307	49307308	C	T	11	GENIC	homozygous	116932015
10	49307729	49307730	G	A	14	GENIC	homozygous	116932017
10	49307882	49307883	T	G	8	GENIC	homozygous	116932019
10	49307886	49307887	T	G	7	GENIC	homozygous	116932021
10	49307935	49307936	C	A	4	GENIC	homozygous	116977682
10	49308590	49308591	G	A	17	GENIC	homozygous	116882360
10	49308856	49308857	C	T	30	GENIC	homozygous	116932023
10	49309328	49309329	G	A	29	GENIC	homozygous	116882366
10	49309430	49309431	C	T	21	GENIC	homozygous	116882368
10	49309589	49309590	C	T	37	GENIC	heterozygous	117993790
10	49309597	49309598	A	G	34	GENIC	homozygous	117009404
10	49309599	49309600	C	T	33	GENIC	homozygous	117009405
10	49309642	49309643	G	C	35	GENIC	heterozygous	118037089
10	49309664	49309665	C	T	32	GENIC	heterozygous	118074762
10	49309675	49309676	C	T	33	GENIC	heterozygous	118037090
10	49309748	49309749	G	A	16	GENIC	homozygous	118037091
10	49309773	49309774	C	T	10	GENIC	homozygous	118037092
10	49309812	49309813	C	T	15	GENIC	heterozygous	118037093
10	49309906	49309907	T	C	14	GENIC	homozygous	118037094
10	49310184	49310185	G	A	9	GENIC	homozygous	117195125
10	49310864	49310865	C	T	19	GENIC	homozygous	116882372
10	49310922	49310923	A	G	29	GENIC	homozygous	116882374
10	49311200	49311201	G	T	21	GENIC	homozygous	116882378
10	49311257	49311258	T	C	27	GENIC	homozygous	116882380
10	49311532	49311533	G	A	20	GENIC	homozygous	116882382
10	49311684	49311685	T	C	11	GENIC	homozygous	116932025
10	49311686	49311687	T	C	11	GENIC	homozygous	116932027
10	49311825	49311826	A	G	26	GENIC	homozygous	116932029
10	49311891	49311892	C	T	31	GENIC	homozygous	116588742
10	49311899	49311900	A	T	33	GENIC	homozygous	116588744
10	49312532	49312533	T	C	17	GENIC	homozygous	116882386
10	49312614	49312615	G	A	16	GENIC	homozygous	116932031