chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	243024699	243024700	A	G	52	GENIC	homozygous	135851842
1	243024920	243024921	T	C	41	GENIC	homozygous	135851843
1	243025642	243025643	C	T	42	GENIC	homozygous	135851844
1	243025772	243025772		T	14	GENIC	homozygous	135469580
1	243026257	243026257		TGT	44	GENIC	possibly homozygous	135469581
1	243027779	243027780	C	T	43	GENIC	homozygous	135851845
1	243027834	243027835	T	C	39	GENIC	homozygous	135851846
1	243027875	243027876	C	T	28	GENIC	homozygous	135851847
1	243027956	243027957	A	G	34	GENIC	homozygous	135851848
1	243028764	243028765	A		44	GENIC	possibly homozygous	135469582
1	243030031	243030032	C	T	48	GENIC	homozygous	135851852
1	243028117	243028118	A	C	38	GENIC	possibly homozygous	135851849
1	243028776	243028777	G	A	47	GENIC	homozygous	135851850
1	243029808	243029809	T	C	48	GENIC	homozygous	135851851
1	243030442	243030443	G	A	48	GENIC	homozygous	135851853
1	243030473	243030474	C	T	41	GENIC	homozygous	135851854
1	243030512	243030513	C	T	36	GENIC	homozygous	135851855
1	243030587	243030588	T	C	39	GENIC	homozygous	135851856
1	243031412	243031413	T		43	GENIC	homozygous	135469583
1	243031453	243031454	A	G	45	GENIC	homozygous	135851857