chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	13261508	13261509	A	G	25	GENIC	homozygous	50363316
12	13262195	13262196	G	C	38	GENIC	homozygous	50363320
12	13262558	13262560	GG	--	20	GENIC	homozygous	50281083
12	13262669	13262670	T	C	27	GENIC	homozygous	50059199
12	13262836	13262837	C	CAA	2	GENIC	heterozygous	50059201
12	13263438	13263439	A	G	54	GENIC	homozygous	50059213
12	13263670	13263671	A	G	14	GENIC	homozygous	50281086
12	13264770	13264771	T	C	63	GENIC	homozygous	50059217
12	13264912	13264913	A	G	31	GENIC	homozygous	50059219
12	13264927	13264928	A	G	33	GENIC	homozygous	50059221
12	13265085	13265086	T	TAA	8	GENIC	possibly homozygous	50059223
12	13265085	13265086	T	TAAA	8	GENIC	heterozygous	50059225
12	13265900	13265901	G	A	30	GENIC	homozygous	50059229
12	13262552	13262553	A	T	20	GENIC	homozygous	50922694
12	13263932	13263961	TTTTTTTTCTTTTTTTTTTTTTTTTTTTT	-----------------------------	4	GENIC	homozygous	50922697
12	13265067	13265068	T	A	15	GENIC	homozygous	50922700
12	13266094	13266125	GGAACAAGGTATGCGCGCGCGCGCGCGCGCA	-------------------------------	12	GENIC	heterozygous	50922702
12	13266666	13266667	C	T	59	GENIC	homozygous	50922705
12	13266088	13266092	AATC	----	1	GENIC	homozygous	50967689