chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	93684887	93684887		TCTCCC	30	GENIC	homozygous	129085962
13	93686104	93686105	C	A	27	GENIC	homozygous	114428986
13	93692716	93692717	G	C	36	GENIC	homozygous	114784774
13	93689855	93689856	C	T	25	GENIC	homozygous	114784768
13	93690812	93690813	G	C	33	GENIC	homozygous	114784770
13	93692503	93692504	G	A	34	GENIC	homozygous	114784772
13	93693097	93693098	C	T	19	GENIC	homozygous	114429012
13	93694590	93694591	G	C	7	GENIC	homozygous	129113978
13	93696170	93696174	AAAT		32	GENIC	homozygous	129085971
13	93697027	93697028	G	A	30	GENIC	homozygous	114784776
13	93697058	93697059	C	A	33	GENIC	homozygous	114429016
13	93697079	93697080	G	A	29	GENIC	homozygous	114429018
13	93697281	93697282	T	G	21	GENIC	homozygous	114429020
13	93697344	93697345	C	T	24	GENIC	homozygous	114429022
13	93697372	93697373	T	C	24	GENIC	homozygous	114429024
13	93697632	93697633	G	A	40	GENIC	homozygous	114784778
13	93698245	93698246	G	A	24	GENIC	homozygous	114784780
13	93698641	93698642	A	G	28	GENIC	homozygous	114429028
13	93698919	93698920	C	A	31	GENIC	homozygous	114784782
13	93699066	93699067	G	A	35	GENIC	homozygous	114784784
13	93699783	93699784	T	C	22	GENIC	homozygous	114429030
13	93703075	93703076	T	C	39	GENIC	homozygous	114784786
13	93703157	93703158	C	T	35	GENIC	homozygous	114429042
13	93704512	93704513	C	T	27	GENIC	homozygous	114429044
13	93707873	93707874	G	A	19	GENIC	homozygous	114784788
13	93709822	93709823	C	A	28	GENIC	homozygous	114784790
13	93710475	93710476	A	G	25	GENIC	homozygous	114429048
13	93711339	93711340	G	A	23	GENIC	homozygous	114429050
13	93714366	93714367	A	T	19	GENIC	homozygous	114429052
13	93714367	93714368	A	T	19	GENIC	homozygous	114429054
13	93696161	93696162	T	A	32	GENIC	homozygous	114650000
13	93708585	93708585		T	22	GENIC	homozygous	129085972
13	93697879	93697889	TGTGTGTGTT		20	GENIC	homozygous	131135267
13	93700856	93700857	A		26	GENIC	homozygous	131135268
13	93710940	93710941	A	T	28	GENIC	homozygous	114930362