chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	26568133	26568134	C	CTGAAT	12	GENIC	homozygous	50439707
12	26568365	26568366	C	T	22	GENIC	homozygous	50439709
12	26570126	26570127	G	A	21	GENIC	homozygous	50439711
12	26570326	26570327	C	CTTCT	8	GENIC	homozygous	50148828
12	26570513	26570514	T	TA	30	GENIC	homozygous	50485147
12	26570772	26570773	T	C	29	GENIC	homozygous	50148832
12	26572368	26572369	T	G	45	GENIC	homozygous	50148836
12	26572442	26572443	C	A	52	GENIC	homozygous	50439713
12	26572549	26572550	T	G	27	GENIC	homozygous	50148838
12	26573490	26573491	G	A	21	GENIC	homozygous	50148840
12	26574205	26574206	G	A	14	GENIC	homozygous	50148846
12	26574226	26574232	ACACAC	------	8	GENIC	heterozygous	50539387
12	26574228	26574232	ACAC	----	8	GENIC	heterozygous	50539388
12	26574368	26574369	T	C	23	GENIC	homozygous	50439715
12	26574819	26574820	C	T	13	GENIC	homozygous	50439717
12	26574836	26574837	T	TTC	14	GENIC	homozygous	50148850
12	26575025	26575026	T	TTGTTTTTTTG	15	GENIC	homozygous	50539389
12	26575336	26575337	T	C	29	GENIC	homozygous	50148858
12	26575938	26575939	T	C	24	GENIC	homozygous	50148860