chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	67414496	67414497	C	T	33	GENIC	homozygous	56929502
4	67414787	67414788	A	-	33	GENIC	homozygous	56929503
4	67415078	67415079	A	G	38	GENIC	homozygous	56929504
4	67415091	67415092	A	T	40	GENIC	homozygous	56929505
4	67415422	67415423	G	C	45	GENIC	homozygous	56929506
4	67416066	67416067	T	TG	9	GENIC	heterozygous	56929507
4	67416067	67416069	CG	--	9	GENIC	possibly homozygous	56929508
4	67416069	67416071	GC	--	15	GENIC	homozygous	56929509
4	67416087	67416088	C	A	22	GENIC	heterozygous	56929510
4	67416214	67416215	T	G	52	GENIC	homozygous	56929511
4	67416294	67416295	A	C	37	GENIC	homozygous	56929512
4	67417298	67417299	G	A	39	GENIC	homozygous	56929513
4	67417311	67417312	A	G	34	GENIC	homozygous	56929514
4	67417354	67417355	C	CT	37	GENIC	homozygous	56929515
4	67418903	67418904	A	-	5	GENIC	homozygous	56929516
4	67419034	67419035	A	T	37	GENIC	homozygous	56929517
4	67419172	67419173	C	CA	12	GENIC	homozygous	56929518
4	67419264	67419265	T	A	34	GENIC	homozygous	56929519
4	67419379	67419380	A	-	2	GENIC	homozygous	56929520
4	67421065	67421066	A	ATC	28	GENIC	heterozygous	56929521
4	67421067	67421068	A	C	30	GENIC	heterozygous	56929522
4	67421067	67421068	A	ATC	26	GENIC	heterozygous	56929523
4	67421120	67421124	TGTA	----	15	GENIC	possibly homozygous	56929524
4	67421888	67421889	C	T	30	GENIC	homozygous	56929525
4	67421900	67421901	T	TAA	20	GENIC	homozygous	56929526
4	67422193	67422194	G	A	33	GENIC	homozygous	56929527
4	67422219	67422220	A	T	35	GENIC	homozygous	56929528
4	67422230	67422231	T	C	32	GENIC	homozygous	56929529
4	67423066	67423067	A	T	45	GENIC	possibly homozygous	56929530