chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	91200933	91200934	C	T	28	GENIC	homozygous	50865244
11	91201159	91201160	T	C	20	GENIC	homozygous	50865245
11	91201739	91201747	TGTGTGTC	--------	18	GENIC	homozygous	50865246
11	91201811	91201812	C	T	22	GENIC	homozygous	50865247
11	91202317	91202318	C	CT	5	GENIC	heterozygous	50865248
11	91202384	91202385	G	A	13	GENIC	homozygous	50865249
11	91202414	91202415	T	C	15	GENIC	homozygous	51135854
11	91202417	91202418	G	A	15	GENIC	homozygous	50865250
11	91202873	91202874	C	CTT	9	GENIC	homozygous	50865251
11	91204849	91204850	T	C	22	GENIC	homozygous	50865254
11	91205643	91205644	G	T	35	GENIC	homozygous	50865255
11	91207359	91207360	T	-	8	GENIC	homozygous	50865260
11	91209928	91209929	G	T	39	GENIC	homozygous	51135857
11	91210545	91210546	A	G	34	GENIC	homozygous	50865261
11	91214208	91214210	AA	--	11	GENIC	possibly homozygous	50898819
11	91214209	91214210	A	-	11	GENIC	heterozygous	50865262
11	91214247	91214257	AAATCCCTGA	----------	9	GENIC	homozygous	50865263
11	91218692	91218693	A	C	26	GENIC	homozygous	50865267
11	91221816	91221817	G	A	39	GENIC	homozygous	50865268
11	91205817	91205818	A	ATTTTTTTT	1	GENIC	homozygous	51193068
11	91205956	91205957	C	CTGTGTG	4	GENIC	homozygous	51193069
11	91217505	91217506	C	A	10	GENIC	possibly homozygous	51193070