chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	73929368	73929369	C	G	48	GENIC	homozygous	114390997
13	73929558	73929559	A	T	36	GENIC	homozygous	114390999
13	73930589	73930590	G	T	50	GENIC	homozygous	114391001
13	73931795	73931796	G	T	60	GENIC	possibly homozygous	114391003
13	73932272	73932273	G	A	50	GENIC	homozygous	114391005
13	73932273	73932274	A	T	51	GENIC	homozygous	114391007
13	73933739	73933740	T	A	77	GENIC	homozygous	114639917
13	73934704	73934705	T	C	60	GENIC	homozygous	114391009
13	73935578	73935579	T	C	35	GENIC	homozygous	114391011
13	73936662	73936663	T	C	38	GENIC	homozygous	114391013
13	73938277	73938278	T	C	65	GENIC	homozygous	114391015
13	73938288	73938289	T	C	65	GENIC	homozygous	114391017
13	73938699	73938700	A	G	66	GENIC	possibly homozygous	114391019
13	73938770	73938771	C	T	66	GENIC	homozygous	114391021
13	73939822	73939823	T	C	63	GENIC	homozygous	114391023
13	73940042	73940043	A	G	51	GENIC	homozygous	114391025
13	73940064	73940065	T	A	56	GENIC	homozygous	114391027
13	73941146	73941147	C	T	61	GENIC	homozygous	114391029
13	73941519	73941520	C	T	61	GENIC	homozygous	118461809
13	73941399	73941400	G	A	52	GENIC	homozygous	118461808