chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	26210014	26210015	T	C	24	GENIC	homozygous	115521496
12	26210021	26210022	C	T	24	GENIC	homozygous	115521497
12	26210609	26210610	G	A	23	GENIC	homozygous	115510398
12	26211184	26211185	A	G	27	GENIC	homozygous	115539992
12	26211502	26211503	C	T	29	GENIC	homozygous	115539994
12	26211978	26211979	C	G	27	GENIC	possibly homozygous	115539996
12	26212044	26212045	A	C	36	GENIC	homozygous	115510399
12	26212146	26212147	G	A	27	GENIC	possibly homozygous	115539998
12	26212252	26212253	G	C	29	GENIC	homozygous	115540000
12	26212474	26212475	A	G	24	GENIC	possibly homozygous	115510402
12	26212486	26212487	C	T	17	GENIC	possibly homozygous	115540002
12	26212757	26212758	G	A	2	GENIC	homozygous	115540004
12	26212774	26212775	G	A	5	GENIC	homozygous	115521500
12	26212965	26212966	A	G	13	GENIC	homozygous	115510410
12	26213095	26213096	T	G	22	GENIC	possibly homozygous	115540006
12	26213111	26213112	G	A	18	GENIC	possibly homozygous	115540008
12	26213153	26213154	T	C	17	GENIC	possibly homozygous	115540010
12	26213185	26213186	A	G	11	GENIC	homozygous	115540012
12	26213187	26213188	C	A	12	GENIC	homozygous	115540014
12	26213252	26213253	A	G	16	GENIC	possibly homozygous	115510412
12	26213435	26213436	G	A	28	GENIC	homozygous	115540016
12	26213571	26213572	A	G	29	GENIC	homozygous	115510415
12	26213987	26213988	A	G	15	GENIC	homozygous	115510417
12	26214584	26214585	C	T	16	GENIC	homozygous	115540018
12	26214655	26214656	A	G	21	GENIC	homozygous	115510418
12	26214656	26214657	T	A	20	GENIC	homozygous	115510419
12	26214662	26214663	C	T	21	GENIC	homozygous	115510420
12	26214673	26214674	G	T	21	GENIC	homozygous	115510421
12	26214709	26214710	C	T	25	GENIC	homozygous	115540020
12	26214740	26214741	T	A	19	GENIC	homozygous	115540022
12	26214843	26214844	C	A	21	GENIC	homozygous	115540024
12	26214854	26214855	A	G	23	GENIC	homozygous	115540026
12	26214891	26214892	C	T	18	GENIC	homozygous	115540028