chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	208628227	208628228	G	C	30	GENIC	homozygous	57066722
4	208628561	208628562	C	T	35	GENIC	homozygous	57066723
4	208630507	208630508	C	CT	9	GENIC	heterozygous	57066724
4	208630507	208630508	C	CTT	9	GENIC	heterozygous	58369179
4	208630759	208630760	C	CG	22	GENIC	homozygous	57066725
4	208632116	208632117	A	-	37	GENIC	homozygous	57363891
4	208632278	208632282	ATTT	----	34	GENIC	homozygous	57066727
4	208632576	208632577	C	CT	30	GENIC	possibly homozygous	57066728
4	208632576	208632577	C	CTT	30	GENIC	heterozygous	58410598
4	208632655	208632656	G	A	23	GENIC	homozygous	57066729
4	208633144	208633145	A	C	28	GENIC	homozygous	57066730
4	208633280	208633281	G	A	30	GENIC	homozygous	57066731
4	208633863	208633864	C	T	23	GENIC	homozygous	57066732
4	208634215	208634216	C	T	27	GENIC	homozygous	57066733
4	208634482	208634483	A	T	20	GENIC	homozygous	57066734
4	208635579	208635580	G	A	27	GENIC	homozygous	57066735
4	208636329	208636330	T	TG	35	GENIC	homozygous	57066736
4	208636397	208636398	T	C	29	GENIC	homozygous	57066737
4	208637238	208637239	T	TGCA	7	GENIC	homozygous	57066738
4	208637478	208637483	TTTTT	-----	21	GENIC	heterozygous	57066739
4	208637479	208637483	TTTT	----	21	GENIC	possibly homozygous	57066740
4	208637781	208637782	C	T	29	GENIC	homozygous	57066741