chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	91597213	91597214	C	A	32	GENIC	homozygous	50866373
11	91597538	91597539	C	T	43	GENIC	homozygous	50866374
11	91598231	91598232	G	T	44	GENIC	homozygous	50866377
11	91598315	91598316	C	T	38	GENIC	homozygous	50866378
11	91598764	91598765	A	T	28	GENIC	homozygous	50866379
11	91599204	91599205	T	C	47	GENIC	homozygous	50866380
11	91599410	91599411	C	T	28	GENIC	homozygous	50866381
11	91599620	91599621	A	G	27	GENIC	homozygous	50866382
11	91599729	91599730	A	-	15	GENIC	possibly homozygous	50866383
11	91599796	91599797	A	G	15	GENIC	homozygous	50866384
11	91599874	91599875	T	C	14	GENIC	homozygous	50866385
11	91600086	91600087	G	A	23	GENIC	homozygous	50866386
11	91600255	91600256	A	G	22	GENIC	homozygous	50866387
11	91600303	91600305	AC	--	13	GENIC	homozygous	50866388
11	91600355	91600356	C	-	13	GENIC	heterozygous	51171356
11	91600469	91600470	T	C	12	GENIC	homozygous	50866389
11	91600484	91600486	CA	--	12	GENIC	homozygous	50866390
11	91600737	91600738	G	A	34	GENIC	homozygous	50866391
11	91600741	91600742	A	G	34	GENIC	homozygous	50866392
11	91602310	91602311	A	C	28	GENIC	homozygous	50866397