chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	208628148	208628149	T	A	26	GENIC	homozygous	58601067
4	208628523	208628524	T	A	28	GENIC	homozygous	58601069
4	208628609	208628610	C	T	21	GENIC	homozygous	58601071
4	208629274	208629275	G	T	16	GENIC	homozygous	58601073
4	208629762	208629763	C	T	29	GENIC	possibly homozygous	58601075
4	208630508	208630510	TT	--	1	GENIC	homozygous	58601077
4	208630997	208630998	T	TAAAAAAA	5	GENIC	homozygous	58601079
4	208631055	208631167	AAGAAACCCAAAGAAGGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCCGAAAAAAAAAAAAAAAAAAAAAA	----------------------------------------------------------------------------------------------------------------	10	GENIC	homozygous	58487559
4	208631189	208631191	GC	--	10	GENIC	homozygous	58601081
4	208631193	208631196	ACA	---	10	GENIC	homozygous	58601083
4	208632116	208632117	A	-	8	GENIC	homozygous	57363891
4	208632278	208632279	A	AT	13	GENIC	homozygous	58302152
4	208632576	208632577	C	CTT	9	GENIC	homozygous	58410598
4	208634482	208634483	A	T	18	GENIC	homozygous	57066734
4	208634588	208634589	T	C	26	GENIC	homozygous	58487563
4	208636329	208636330	T	TG	19	GENIC	homozygous	57066736
4	208636397	208636398	T	C	23	GENIC	homozygous	57066737
4	208636565	208636566	T	G	24	GENIC	homozygous	58601085
4	208636984	208636985	A	G	32	GENIC	homozygous	58601087
4	208637413	208637414	C	CT	14	GENIC	possibly homozygous	58601089
4	208637477	208637478	C	CTTT	8	GENIC	possibly homozygous	58410599