chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	37267036	37267037	G	A	18	GENIC	homozygous	114315637
13	37269288	37269289	C	T	26	GENIC	homozygous	114529303
13	37270506	37270507	G	A	24	GENIC	homozygous	114315638
13	37271471	37271472	A	G	25	GENIC	homozygous	114315639
13	37273458	37273459	A	T	19	GENIC	homozygous	114315640
13	37274880	37274881	C	T	21	GENIC	homozygous	114315641
13	37276119	37276120	C	T	26	GENIC	homozygous	114315642
13	37277127	37277128	A	G	31	GENIC	homozygous	114315643
13	37280778	37280779	G	C	30	GENIC	homozygous	114315644
13	37281124	37281125	T	C	20	GENIC	homozygous	114315645
13	37281255	37281256	A	C	33	GENIC	homozygous	114315646
13	37281809	37281810	T	C	15	GENIC	possibly homozygous	114529309
13	37285151	37285152	A	G	35	GENIC	possibly homozygous	114315647
13	37285877	37285878	A	G	28	GENIC	homozygous	114315648
13	37285907	37285908	A	C	28	GENIC	homozygous	114315649
13	37287806	37287807	T	C	19	GENIC	homozygous	114315650
13	37288883	37288884	A	G	20	GENIC	homozygous	114315652
13	37288989	37288990	T	A	18	GENIC	possibly homozygous	115178229
13	37289139	37289140	T	C	23	GENIC	homozygous	114315653
13	37289535	37289536	T	C	12	GENIC	homozygous	114315654
13	37289536	37289537	T	A	12	GENIC	homozygous	114315655
13	37289537	37289538	T	G	14	GENIC	homozygous	114315656
13	37291526	37291527	A	G	30	GENIC	homozygous	114315657
13	37291956	37291957	C	T	22	GENIC	possibly homozygous	114315658