chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	142166699	142166700	T	TATC	24	GENIC	homozygous	57504085
4	142167192	142167193	G	-	13	GENIC	possibly homozygous	57504087
4	142169634	142169635	C	T	24	GENIC	possibly homozygous	57504089
4	142169775	142169776	T	TAAATAAACAAATC	12	GENIC	homozygous	57504091
4	142169780	142169781	A	ACAAATCTT	15	GENIC	possibly homozygous	57504093
4	142170328	142170329	G	A	18	GENIC	homozygous	57504095
4	142170640	142170641	C	T	30	GENIC	homozygous	57504097
4	142171157	142171158	G	C	35	GENIC	homozygous	57504099
4	142173153	142173154	A	AAGAGAG	9	GENIC	heterozygous	57504101
4	142173956	142173957	A	G	35	GENIC	homozygous	57504103
4	142176618	142176619	T	C	29	GENIC	homozygous	56960120
4	142173153	142173154	A	AAGAG	9	GENIC	heterozygous	56960117
4	142176227	142176228	C	CT	13	GENIC	possibly homozygous	56960118
4	142176273	142176274	T	TTG	4	GENIC	homozygous	56960119
4	142176642	142176643	G	C	28	GENIC	homozygous	57504105
4	142177386	142177387	T	A	34	GENIC	homozygous	56960121
4	142177528	142177529	C	-	16	GENIC	homozygous	57504107
4	142177593	142177597	TTTA	----	5	GENIC	heterozygous	56960122
4	142177844	142177845	A	ATGTG	17	GENIC	homozygous	57342145
4	142178054	142178055	T	TTA	8	GENIC	homozygous	56960126