chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	42367264	42367265	T	C	24	GENIC	homozygous	50745732
13	42390622	42390623	G	-	22	GENIC	homozygous	49736371
13	42390650	42390651	T	C	23	GENIC	homozygous	49939318
13	42390651	42390652	T	A	23	GENIC	homozygous	49939319
13	42390652	42390653	T	G	23	GENIC	homozygous	49939320
13	42390657	42390658	C	-	20	GENIC	homozygous	49736372
13	42390663	42390664	G	-	21	GENIC	homozygous	49736373
13	42390667	42390668	G	-	17	GENIC	homozygous	49736374
13	42390753	42390754	C	-	13	GENIC	homozygous	49736375
13	42390786	42390787	A	-	6	GENIC	homozygous	49736376
13	42390810	42390811	T	-	8	GENIC	homozygous	49736377
13	42391118	42391119	A	-	9	GENIC	heterozygous	50612317
13	42392811	42392812	G	GT	22	GENIC	homozygous	49736383
13	42392912	42392913	C	CTG	4	GENIC	heterozygous	49736384