chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	93983009	93983010	G	A	32	GENIC	homozygous	51745915
10	93984387	93984388	T	TC	5	GENIC	homozygous	51745917
10	93984539	93984540	G	T	16	GENIC	homozygous	51745919
10	93984905	93984906	C	A	21	GENIC	homozygous	51745921
10	93986802	93986803	A	C	9	GENIC	homozygous	51745923
10	93987006	93987008	GT	--	15	GENIC	heterozygous	51547906
10	93990522	93990523	G	A	19	GENIC	homozygous	51745925
10	93991439	93991440	G	A	27	GENIC	homozygous	51547910
10	93993106	93993107	A	G	31	GENIC	homozygous	51745927
10	93993150	93993151	G	C	31	GENIC	homozygous	51745929
10	93993388	93993389	C	T	29	GENIC	homozygous	51547914
10	93993419	93993420	C	T	28	GENIC	homozygous	51745931
10	93993693	93993694	A	G	26	GENIC	homozygous	51547915
10	93994217	93994218	T	TC	25	GENIC	homozygous	51547917
10	93995913	93995914	C	T	28	GENIC	homozygous	51745933
10	93997035	93997036	G	GAC	21	GENIC	heterozygous	51547925
10	93998649	93998650	C	T	27	GENIC	homozygous	51745935
10	93999785	93999786	G	A	18	GENIC	homozygous	51745937
10	94000280	94000281	C	T	21	GENIC	homozygous	51745939
10	94001690	94001691	T	C	41	GENIC	homozygous	51547931
10	94002094	94002095	T	C	34	GENIC	homozygous	51547932
10	94002200	94002201	A	G	42	GENIC	homozygous	51547933
10	94004374	94004375	C	T	22	GENIC	homozygous	51745941
10	93993547	93993548	C	CTTTTT	13	GENIC	homozygous	52398947