chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	96820943	96820944	C	G	12	GENIC	homozygous	114433046
13	96820944	96820945	T	C	12	GENIC	homozygous	114433048
13	96820964	96820965	C	T	12	GENIC	homozygous	114433050
13	96821569	96821570	G	T	12	GENIC	homozygous	114433052
13	96821570	96821571	T	G	12	GENIC	homozygous	114433054
13	96821685	96821686	C	T	15	GENIC	homozygous	114433056
13	96821891	96821892	A	G	14	GENIC	homozygous	114433058
13	96876528	96876529	C	G	20	GENIC	homozygous	114583021
13	96909996	96909997	T	G	10	GENIC	homozygous	114583027
13	96910205	96910206	C	T	12	GENIC	homozygous	114433407
13	96910349	96910350	T	G	5	GENIC	homozygous	115079024
13	96927251	96927252	C	A	20	GENIC	homozygous	114433517
13	96927372	96927373	C	G	18	GENIC	homozygous	114433519
13	96973702	96973703	A	C	14	GENIC	heterozygous	115079026
13	96995984	96995985	C	A	18	GENIC	homozygous	114650377
13	97013590	97013591	C	T	27	GENIC	homozygous	114583031
13	97017841	97017842	C	T	18	GENIC	homozygous	114832664
13	97020209	97020210	C	A	17	GENIC	homozygous	114433695
13	97020212	97020213	C	A	17	GENIC	homozygous	114583035
13	97020215	97020216	C	A	17	GENIC	homozygous	114583037
13	97020232	97020233	T	A	19	GENIC	homozygous	114583039
13	97053919	97053920	T	C	12	GENIC	homozygous	114433785
13	97053921	97053922	T	C	12	GENIC	homozygous	114433787
13	97053928	97053929	T	A	12	GENIC	homozygous	114650385
13	97053956	97053957	T	A	17	GENIC	homozygous	114650387
13	97082614	97082615	G	A	12	GENIC	heterozygous	115079028