chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	142392695	142392696	G	C	21	GENIC	homozygous	56960492
4	142392718	142392719	T	TTGA	18	GENIC	homozygous	56960493
4	142394432	142394433	T	C	32	GENIC	homozygous	56960495
4	142395616	142395618	GG	--	14	GENIC	heterozygous	56960496
4	142395617	142395618	G	-	14	GENIC	possibly homozygous	56960497
4	142395648	142395649	A	G	29	GENIC	homozygous	56960498
4	142396752	142396753	C	T	37	GENIC	homozygous	56960500
4	142397545	142397546	C	T	36	GENIC	homozygous	56960501
4	142399124	142399125	G	C	31	GENIC	homozygous	56960502
4	142405088	142405089	T	C	27	GENIC	homozygous	56960503
4	142405810	142405811	A	-	23	GENIC	possibly homozygous	56960504
4	142413456	142413457	C	T	40	GENIC	homozygous	56960505
4	142415536	142415537	G	T	30	GENIC	homozygous	56960506
4	142415551	142415552	C	T	30	GENIC	homozygous	56960507