chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	26090202	26090203	C	G	13	GENIC	homozygous	50145588
12	26090236	26090237	C	CTTCTGAGAAAA	12	GENIC	homozygous	50372894
12	26090860	26090869	TGTGTGTGT	---------	5	GENIC	homozygous	50372900
12	26090866	26090867	T	-	7	GENIC	heterozygous	50372902
12	26090868	26090869	T	-	10	GENIC	heterozygous	50372903
12	26091890	26091891	C	T	25	GENIC	homozygous	50404486
12	26092144	26092145	G	A	42	GENIC	heterozygous	50404488
12	26092167	26092168	G	A	18	GENIC	heterozygous	50404490
12	26092277	26092278	A	T	24	GENIC	homozygous	50404492
12	26092412	26092413	G	T	30	GENIC	homozygous	50372927
12	26092745	26092746	C	A	21	GENIC	homozygous	50404494
12	26092803	26092804	G	A	29	GENIC	homozygous	50404496
12	26093060	26093061	A	C	29	GENIC	homozygous	50372944
12	26093660	26093662	TC	--	29	GENIC	homozygous	50404498
12	26094193	26094194	A	C	21	GENIC	heterozygous	50404500
12	26094500	26094501	G	A	22	GENIC	homozygous	50404502
12	26094523	26094524	T	C	19	GENIC	homozygous	50404504
12	26094749	26094750	C	T	39	GENIC	homozygous	50404506
12	26094783	26094784	A	G	41	GENIC	homozygous	50404508
12	26095149	26095150	G	GAA	14	GENIC	heterozygous	50145593
12	26095149	26095150	G	GA	14	GENIC	heterozygous	50145595
12	26095167	26095168	C	-	20	GENIC	homozygous	50372980
12	26095171	26095173	AC	--	20	GENIC	homozygous	50372982
12	26095379	26095380	T	C	27	GENIC	homozygous	50372986
12	26096368	26096369	G	A	13	GENIC	homozygous	50404510
12	26096526	26096527	A	T	19	GENIC	homozygous	50373010
12	26096910	26096911	T	A	37	GENIC	homozygous	50373020
12	26097621	26097625	GTGA	----	28	GENIC	homozygous	50145603
12	26098586	26098587	C	T	19	GENIC	homozygous	50404512