chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	24182524	24182525	T	C	15	GENIC	homozygous	50132057
12	24183219	24183220	A	G	22	GENIC	homozygous	50132059
12	24183719	24183720	C	T	27	GENIC	homozygous	50132061
12	24183969	24183970	C	T	17	GENIC	homozygous	50132063
12	24184022	24184023	A	AT	21	GENIC	homozygous	50132065
12	24184097	24184098	G	A	20	GENIC	homozygous	50132067
12	24184103	24184104	G	C	21	GENIC	homozygous	50538432
12	24184105	24184106	C	T	22	GENIC	homozygous	50538433
12	24184159	24184160	T	TGCATG	17	GENIC	homozygous	50132069
12	24184335	24184336	T	A	21	GENIC	homozygous	50132071
12	24184359	24184360	G	GTGTGTT	13	GENIC	homozygous	50538434
12	24184369	24184370	T	C	8	GENIC	homozygous	50132077
12	24184375	24184376	G	T	10	GENIC	homozygous	50132079
12	24184381	24184382	G	C	13	GENIC	homozygous	50132081
12	24184479	24184480	G	C	14	GENIC	homozygous	50538435
12	24184487	24184488	C	G	12	GENIC	homozygous	50132083
12	24184491	24184492	C	T	12	GENIC	homozygous	50132085
12	24184501	24184502	G	GTGTC	9	GENIC	homozygous	50538436
12	24184532	24184534	TG	--	14	GENIC	possibly homozygous	50132087
12	24184943	24184944	C	CTG	22	GENIC	homozygous	50132104
12	24184975	24184976	G	T	10	GENIC	homozygous	50132108
12	24185177	24185178	C	T	36	GENIC	homozygous	50132112
12	24185634	24185635	C	CAAAAA	8	GENIC	heterozygous	50132116
12	24185634	24185635	C	CAAAA	8	GENIC	heterozygous	50538437
12	24185634	24185635	C	CAAAAAAAAAAAAA	8	GENIC	heterozygous	50538438
12	24184987	24184988	C	CTGTG	10	GENIC	homozygous	50561447