chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	24182524	24182525	T	C	39	GENIC	homozygous	50132057
12	24183219	24183220	A	G	44	GENIC	homozygous	50132059
12	24183719	24183720	C	T	47	GENIC	homozygous	50132061
12	24183969	24183970	C	T	44	GENIC	homozygous	50132063
12	24184022	24184023	A	AT	38	GENIC	homozygous	50132065
12	24184097	24184098	G	A	31	GENIC	homozygous	50132067
12	24184159	24184160	T	TGCATG	27	GENIC	homozygous	50132069
12	24184335	24184336	T	A	41	GENIC	homozygous	50132071
12	24184342	24184346	TGTG	----	16	GENIC	possibly homozygous	50132073
12	24184369	24184370	T	C	26	GENIC	heterozygous	50132077
12	24184375	24184376	G	T	51	GENIC	heterozygous	50132079
12	24184381	24184382	G	C	51	GENIC	heterozygous	50132081
12	24184487	24184488	C	G	33	GENIC	heterozygous	50132083
12	24184491	24184492	C	T	18	GENIC	heterozygous	50132085
12	24184532	24184534	TG	--	33	GENIC	heterozygous	50132087
12	24184547	24184548	G	C	101	GENIC	heterozygous	50132089
12	24184595	24184596	G	A	176	GENIC	heterozygous	50132091
12	24184612	24184616	TGTC	----	86	GENIC	heterozygous	50132094
12	24184633	24184634	A	G	204	GENIC	heterozygous	50132096
12	24184668	24184670	TC	--	113	GENIC	heterozygous	50132098
12	24184673	24184674	C	G	202	GENIC	heterozygous	50132100
12	24184808	24184812	TCTC	----	43	GENIC	homozygous	50132102
12	24184943	24184944	C	CTG	34	GENIC	possibly homozygous	50132104
12	24184958	24184960	TC	--	38	GENIC	heterozygous	50132106
12	24184975	24184976	G	T	50	GENIC	heterozygous	50132108
12	24184995	24184999	GTGC	----	38	GENIC	heterozygous	50132110
12	24185177	24185178	C	T	48	GENIC	homozygous	50132112
12	24185634	24185635	C	CAAAAA	3	GENIC	homozygous	50132116
12	24185649	24185650	G	A	18	GENIC	heterozygous	50292687
12	24184735	24184736	G	A	96	GENIC	heterozygous	50371473