chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	96820943	96820944	C	G	22	GENIC	homozygous	114433046
13	96820944	96820945	T	C	22	GENIC	homozygous	114433048
13	96820964	96820965	C	T	22	GENIC	homozygous	114433050
13	96821569	96821570	G	T	18	GENIC	homozygous	114433052
13	96821570	96821571	T	G	18	GENIC	homozygous	114433054
13	96821685	96821686	C	T	20	GENIC	homozygous	114433056
13	96821891	96821892	A	G	39	GENIC	homozygous	114433058
13	96830895	96830896	T	C	24	GENIC	homozygous	114433076
13	96839414	96839415	A	T	44	GENIC	homozygous	114583013
13	96830896	96830897	C	T	22	GENIC	homozygous	114832660
13	96876528	96876529	C	G	25	GENIC	homozygous	114583021
13	96909996	96909997	T	G	31	GENIC	homozygous	114583027
13	96910205	96910206	C	T	30	GENIC	homozygous	114433407
13	96910410	96910411	T	G	1	GENIC	homozygous	114832662
13	96927372	96927373	C	G	29	GENIC	homozygous	114433519
13	96994553	96994554	C	A	18	GENIC	homozygous	114433629
13	96994557	96994558	A	C	18	GENIC	homozygous	114433631
13	96995984	96995985	C	A	7	GENIC	homozygous	114650377
13	97013590	97013591	C	T	28	GENIC	homozygous	114583031
13	97017841	97017842	C	T	27	GENIC	homozygous	114832664
13	97053919	97053920	T	C	37	GENIC	homozygous	114433785
13	97053921	97053922	T	C	34	GENIC	homozygous	114433787
13	97053928	97053929	T	A	34	GENIC	homozygous	114650385
13	97053956	97053957	T	A	29	GENIC	homozygous	114650387