chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	24182524	24182525	T	C	26	GENIC	homozygous	50132057
12	24183219	24183220	A	G	19	GENIC	homozygous	50132059
12	24183719	24183720	C	T	23	GENIC	homozygous	50132061
12	24183969	24183970	C	T	14	GENIC	homozygous	50132063
12	24184022	24184023	A	AT	23	GENIC	homozygous	50132065
12	24184097	24184098	G	A	16	GENIC	homozygous	50132067
12	24184159	24184160	T	TGCATG	19	GENIC	homozygous	50132069
12	24184335	24184336	T	A	8	GENIC	homozygous	50132071
12	24184342	24184346	TGTG	----	4	GENIC	heterozygous	50132073
12	24184359	24184360	G	T	14	GENIC	heterozygous	50132075
12	24184369	24184370	T	C	13	GENIC	heterozygous	50132077
12	24184375	24184376	G	T	17	GENIC	heterozygous	50132079
12	24184381	24184382	G	C	16	GENIC	heterozygous	50132081
12	24184487	24184488	C	G	16	GENIC	heterozygous	50132083
12	24184491	24184492	C	T	13	GENIC	heterozygous	50132085
12	24184532	24184534	TG	--	8	GENIC	heterozygous	50132087
12	24184547	24184548	G	C	30	GENIC	heterozygous	50132089
12	24184612	24184616	TGTC	----	40	GENIC	heterozygous	50132094
12	24184633	24184634	A	G	79	GENIC	heterozygous	50132096
12	24184668	24184670	TC	--	46	GENIC	heterozygous	50132098
12	24184673	24184674	C	G	78	GENIC	heterozygous	50132100
12	24184808	24184812	TCTC	----	16	GENIC	homozygous	50132102
12	24184943	24184944	C	CTG	24	GENIC	homozygous	50132104
12	24184958	24184960	TC	--	28	GENIC	heterozygous	50132106
12	24184975	24184976	G	T	37	GENIC	heterozygous	50132108
12	24184995	24184999	GTGC	----	27	GENIC	possibly homozygous	50132110
12	24185177	24185178	C	T	21	GENIC	homozygous	50132112
12	24185634	24185635	C	CAAAAA	5	GENIC	homozygous	50132116
12	24185649	24185650	G	A	15	GENIC	heterozygous	50292687