chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	135690359	135690360	C	T	12	GENIC	homozygous	56939037
4	135690889	135690890	G	A	9	GENIC	homozygous	56939038
4	135691660	135691661	T	A	25	GENIC	homozygous	56939040
4	135691722	135691723	G	A	22	GENIC	homozygous	56939041
4	135692567	135692568	G	T	25	GENIC	homozygous	56939042
4	135692820	135692823	CAG	---	28	GENIC	homozygous	58282885
4	135692823	135692824	A	AC	27	GENIC	homozygous	58282887
4	135694573	135694574	G	A	21	GENIC	homozygous	56939045
4	135694723	135694724	G	GT	14	GENIC	possibly homozygous	56939046
4	135695018	135695019	G	C	30	GENIC	homozygous	56939047
4	135695676	135695677	A	G	18	GENIC	homozygous	56939048
4	135696770	135696771	T	C	29	GENIC	homozygous	56939049
4	135697479	135697480	C	T	28	GENIC	homozygous	56939050
4	135697528	135697529	T	C	28	GENIC	homozygous	56939051
4	135697955	135697956	C	T	24	GENIC	homozygous	56939052
4	135697974	135697975	C	T	22	GENIC	homozygous	56939053
4	135699720	135699721	A	G	29	GENIC	homozygous	56939054
4	135700489	135700490	G	A	26	GENIC	homozygous	56939055
4	135701491	135701492	C	-	6	GENIC	heterozygous	59059139
4	135702788	135702789	G	GGGCTTCTAGGCGCATGCCTGGTGA	24	GENIC	homozygous	56939058
4	135703099	135703100	T	C	26	GENIC	homozygous	56939059
4	135704927	135704928	G	A	24	GENIC	homozygous	56939061