chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	25987637	25987638	C	T	24	GENIC	homozygous	50297802
12	25987759	25987760	C	G	29	GENIC	homozygous	50144326
12	25988026	25988027	A	-	26	GENIC	homozygous	50297804
12	25989196	25989197	T	C	20	GENIC	homozygous	50144329
12	25989352	25989353	C	T	37	GENIC	homozygous	50144331
12	25990274	25990275	C	T	42	GENIC	possibly homozygous	50297806
12	25990746	25990748	AA	--	21	GENIC	heterozygous	50144333
12	25990747	25990748	A	-	21	GENIC	heterozygous	50144335
12	25991726	25991727	G	T	21	GENIC	homozygous	50297808
12	25992296	25992297	G	GCTTTCTTTCTTTCTTT	4	GENIC	homozygous	50539162
12	25994548	25994549	T	C	17	GENIC	homozygous	50144349
12	25995284	25995285	C	T	27	GENIC	homozygous	50297810