chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	26209487	26209488	A	G	20	GENIC	homozygous	115510397
12	26210609	26210610	G	A	28	GENIC	homozygous	115510398
12	26212044	26212045	A	C	23	GENIC	homozygous	115510399
12	26212243	26212244	T	G	27	GENIC	homozygous	115510400
12	26212449	26212450	C	A	21	GENIC	homozygous	115510401
12	26212474	26212475	A	G	17	GENIC	homozygous	115510402
12	26212844	26212845	C	T	8	GENIC	homozygous	115510403
12	26212881	26212882	C	T	16	GENIC	homozygous	115510404
12	26212899	26212900	C	T	15	GENIC	homozygous	115510405
12	26212924	26212925	C	T	18	GENIC	homozygous	115510406
12	26212938	26212939	C	T	23	GENIC	homozygous	115510407
12	26212955	26212956	T	C	20	GENIC	homozygous	115510408
12	26212956	26212957	G	A	20	GENIC	homozygous	115510409
12	26212965	26212966	A	G	20	GENIC	homozygous	115510410
12	26213001	26213002	A	C	19	GENIC	homozygous	115510411
12	26213252	26213253	A	G	13	GENIC	homozygous	115510412
12	26213454	26213455	C	T	15	GENIC	homozygous	115510413
12	26213487	26213488	T	A	18	GENIC	homozygous	115510414
12	26213571	26213572	A	G	22	GENIC	homozygous	115510415
12	26213647	26213648	A	G	31	GENIC	homozygous	115510416
12	26213987	26213988	A	G	25	GENIC	homozygous	115510417
12	26214655	26214656	A	G	18	GENIC	homozygous	115510418
12	26214656	26214657	T	A	17	GENIC	homozygous	115510419
12	26214662	26214663	C	T	18	GENIC	homozygous	115510420
12	26214673	26214674	G	T	15	GENIC	homozygous	115510421