chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	24182524	24182525	T	C	11	GENIC	homozygous	50132057
12	24183219	24183220	A	G	27	GENIC	possibly homozygous	50132059
12	24183719	24183720	C	T	13	GENIC	heterozygous	50132061
12	24183969	24183970	C	T	18	GENIC	possibly homozygous	50132063
12	24184022	24184023	A	AT	11	GENIC	homozygous	50132065
12	24184097	24184098	G	A	6	GENIC	homozygous	50132067
12	24184103	24184104	G	C	9	GENIC	homozygous	50538432
12	24184105	24184106	C	T	9	GENIC	homozygous	50538433
12	24184159	24184160	T	TGCATG	3	GENIC	heterozygous	50132069
12	24184335	24184336	T	A	7	GENIC	homozygous	50132071
12	24184359	24184360	G	GTGTGTT	2	GENIC	homozygous	50538434
12	24184381	24184382	G	C	1	GENIC	homozygous	50132081
12	24185177	24185178	C	T	15	GENIC	possibly homozygous	50132112
12	24185634	24185635	C	CAAAAAAAAAAAAA	1	GENIC	homozygous	50538438