chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	107942101	107942102	T	TG	24	GENIC	homozygous	49874627
13	107942584	107942585	G	GT	18	GENIC	homozygous	49874628
13	107943147	107943148	T	TCCTCCTCCTCCTCCCC	5	GENIC	homozygous	50535546
13	107945768	107945769	A	AAAAG	8	GENIC	possibly homozygous	50535548
13	107954833	107954835	CA	--	21	GENIC	heterozygous	50535550
13	107959540	107959541	C	-	21	GENIC	heterozygous	50535552
13	107963958	107963959	T	TCCACATAG	2	GENIC	homozygous	50535554
13	107963964	107963965	C	CTCACAA	2	GENIC	homozygous	50535556
13	107963966	107963967	C	CAT	2	GENIC	homozygous	50535558
13	107963969	107963970	G	GTAATAAATATATCTTA	2	GENIC	homozygous	50535560
13	107964242	107964243	G	GA	11	GENIC	heterozygous	50535562