chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	93686104	93686105	C	A	11	GENIC	homozygous	114428986
13	93687613	93687614	A	G	18	GENIC	homozygous	126070851
13	93687825	93687826	G	T	18	GENIC	homozygous	126070852
13	93689855	93689856	C	T	10	GENIC	homozygous	114784768
13	93692716	93692717	G	C	24	GENIC	homozygous	114784774
13	93693097	93693098	C	T	10	GENIC	homozygous	114429012
13	93693888	93693889	G	A	16	GENIC	homozygous	114970949
13	93696841	93696842	G	A	7	GENIC	homozygous	114970953
13	93697058	93697059	C	A	16	GENIC	homozygous	114429016
13	93697281	93697282	T	G	16	GENIC	homozygous	114429020
13	93697372	93697373	T	C	17	GENIC	homozygous	114429024
13	93697632	93697633	G	A	12	GENIC	homozygous	114784778
13	93698245	93698246	G	A	11	GENIC	homozygous	114784780
13	93698641	93698642	A	G	31	GENIC	homozygous	114429028
13	93698919	93698920	C	A	21	GENIC	homozygous	114784782
13	93699066	93699067	G	A	12	GENIC	homozygous	114784784
13	93699783	93699784	T	C	16	GENIC	homozygous	114429030
13	93699837	93699838	C	G	9	GENIC	heterozygous	114950322
13	93702692	93702693	C	T	6	GENIC	homozygous	114970955
13	93703075	93703076	T	C	14	GENIC	homozygous	114784786
13	93703157	93703158	C	T	22	GENIC	homozygous	114429042
13	93704512	93704513	C	T	5	GENIC	homozygous	114429044
13	93707570	93707571	C	T	22	GENIC	homozygous	114970957
13	93709812	93709813	A	C	17	GENIC	homozygous	114970959
13	93710475	93710476	A	G	18	GENIC	homozygous	114429048
13	93710940	93710941	A	T	9	GENIC	homozygous	114930362
13	93711339	93711340	G	A	12	GENIC	homozygous	114429050