chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	236414541	236414542	T	C	32	GENIC	homozygous	110319408
2	236414795	236414796	C	T	13	GENIC	homozygous	110319410
2	236414984	236414985	A	G	16	GENIC	homozygous	110319412
2	236415546	236415547	C	G	16	GENIC	homozygous	110319414
2	236415949	236415950	A	G	13	GENIC	homozygous	110319416
2	236416121	236416122	A	C	27	GENIC	homozygous	110319418
2	236416328	236416329	T	C	21	GENIC	homozygous	110319420
2	236416658	236416659	T	G	16	GENIC	homozygous	110319422
2	236416686	236416687	T	C	14	GENIC	homozygous	110319424
2	236416748	236416749	A	G	13	GENIC	homozygous	110319426
2	236417786	236417787	T	C	14	GENIC	homozygous	110319428
2	236418027	236418028	G	A	23	GENIC	homozygous	110319430
2	236419009	236419010	T	A	22	GENIC	homozygous	110319432
2	236419222	236419223	C	T	22	GENIC	homozygous	110319434
2	236419586	236419587	T	C	20	GENIC	homozygous	110319436
2	236421368	236421369	T	C	33	GENIC	homozygous	110319440
2	236425587	236425588	T	C	14	GENIC	homozygous	110319470
2	236425967	236425968	A	G	20	GENIC	homozygous	110319472
2	236426954	236426955	C	G	18	GENIC	homozygous	110319474
2	236429313	236429314	C	T	23	GENIC	homozygous	110319489
2	236429485	236429486	T	C	27	GENIC	homozygous	110319491
2	236429889	236429890	C	T	20	GENIC	homozygous	110319493