chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	93684887	93684887		TCTCCC	13	GENIC	homozygous	129085962
13	93686104	93686105	C	A	17	GENIC	homozygous	114428986
13	93692716	93692717	G	C	26	GENIC	homozygous	114784774
13	93689855	93689856	C	T	18	GENIC	homozygous	114784768
13	93693097	93693098	C	T	26	GENIC	homozygous	114429012
13	93693888	93693889	G	A	20	GENIC	homozygous	114970949
13	93696161	93696162	T	A	17	GENIC	homozygous	114650000
13	93696761	93696762	C	T	19	GENIC	homozygous	114970951
13	93696841	93696842	G	A	23	GENIC	possibly homozygous	114970953
13	93697058	93697059	C	A	19	GENIC	homozygous	114429016
13	93697281	93697282	T	G	21	GENIC	homozygous	114429020
13	93697372	93697373	T	C	24	GENIC	homozygous	114429024
13	93697632	93697633	G	A	28	GENIC	homozygous	114784778
13	93698245	93698246	G	A	20	GENIC	homozygous	114784780
13	93698641	93698642	A	G	24	GENIC	homozygous	114429028
13	93698919	93698920	C	A	19	GENIC	homozygous	114784782
13	93699066	93699067	G	A	17	GENIC	homozygous	114784784
13	93699783	93699784	T	C	17	GENIC	homozygous	114429030
13	93699833	93699835	CT		13	GENIC	homozygous	134595735
13	93702692	93702693	C	T	13	GENIC	homozygous	114970955
13	93703075	93703076	T	C	18	GENIC	homozygous	114784786
13	93703157	93703158	C	T	20	GENIC	homozygous	114429042
13	93704512	93704513	C	T	30	GENIC	homozygous	114429044
13	93707570	93707571	C	T	24	GENIC	homozygous	114970957
13	93708585	93708585		T	17	GENIC	homozygous	129085972
13	93709812	93709813	A	C	26	GENIC	homozygous	114970959
13	93710475	93710476	A	G	30	GENIC	homozygous	114429048
13	93697436	93697437	C		27	GENIC	homozygous	131135266
13	93711339	93711340	G	A	26	GENIC	homozygous	114429050
13	93714367	93714368	A	T	19	GENIC	homozygous	114429054
13	93697879	93697889	TGTGTGTGTT		22	GENIC	homozygous	131135267
13	93700856	93700857	A		19	GENIC	homozygous	131135268
13	93708795	93708795		T	27	GENIC	possibly homozygous	131135269
13	93710940	93710941	A	T	25	GENIC	homozygous	114930362