chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	26568133	26568134	C	CTGAAT	4	GENIC	homozygous	50439707
12	26568365	26568366	C	T	2	GENIC	heterozygous	50439709
12	26570126	26570127	G	A	5	GENIC	heterozygous	50439711
12	26570513	26570514	T	TA	10	GENIC	homozygous	50485147
12	26570772	26570773	T	C	17	GENIC	possibly homozygous	50148832
12	26572368	26572369	T	G	7	GENIC	homozygous	50148836
12	26572442	26572443	C	A	6	GENIC	homozygous	50439713
12	26572549	26572550	T	G	9	GENIC	homozygous	50148838
12	26573490	26573491	G	A	10	GENIC	heterozygous	50148840
12	26574205	26574206	G	A	16	GENIC	homozygous	50148846
12	26574368	26574369	T	C	11	GENIC	possibly homozygous	50439715
12	26574819	26574820	C	T	5	GENIC	homozygous	50439717
12	26574836	26574837	T	TTC	3	GENIC	homozygous	50148850
12	26575336	26575337	T	C	16	GENIC	possibly homozygous	50148858
12	26575938	26575939	T	C	5	GENIC	heterozygous	50148860