chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	30630011	30630012	C	T	45	GENIC	homozygous	50715241
11	30631069	30631070	G	A	57	GENIC	homozygous	50715242
11	30631528	30631529	C	T	62	GENIC	homozygous	50715243
11	30632506	30632507	C	G	37	GENIC	homozygous	50715244
11	30633295	30633296	G	A	62	GENIC	possibly homozygous	50715245
11	30633306	30633307	T	C	65	GENIC	homozygous	50715246
11	30633698	30633699	A	C	56	GENIC	homozygous	50715247
11	30633972	30633976	GTGT	----	3	GENIC	homozygous	50715248
11	30634214	30634215	T	C	57	GENIC	homozygous	50715249
11	30634652	30634653	A	G	68	GENIC	homozygous	50715250
11	30634972	30634973	T	C	55	GENIC	homozygous	50715251
11	30635592	30635593	C	T	57	GENIC	homozygous	50715252
11	30635941	30635942	A	C	84	GENIC	homozygous	50715253
11	30636551	30636552	A	AAATTTTCTCT	24	GENIC	homozygous	50715254
11	30636710	30636711	T	TCA	39	GENIC	homozygous	50715255
11	30637045	30637046	G	A	60	GENIC	homozygous	50715256
11	30637641	30637642	A	G	43	GENIC	homozygous	50715257
11	30637964	30637965	C	T	63	GENIC	homozygous	50715258
11	30638108	30638109	G	A	51	GENIC	possibly homozygous	50715259
11	30638596	30638597	A	G	51	GENIC	homozygous	50715260
11	30638986	30638987	T	-	33	GENIC	heterozygous	50715261
11	30638987	30638988	G	GAAAGAGCCAAACAAGGCCCTGCA	31	GENIC	homozygous	50715262
11	30639139	30639140	A	G	73	GENIC	homozygous	50715263
11	30640099	30640100	A	G	66	GENIC	homozygous	50715264
11	30640558	30640559	G	A	51	GENIC	homozygous	50715265
11	30640681	30640682	A	AT	30	GENIC	homozygous	50715266
11	30640791	30640792	C	G	47	GENIC	homozygous	50715267
11	30640936	30640937	T	TAACCACTGACTC	20	GENIC	homozygous	50715268
11	30641080	30641081	A	AG	14	GENIC	heterozygous	50715269
11	30641308	30641318	AATTGAGCTA	----------	9	GENIC	homozygous	50715270
11	30641331	30641333	AA	--	19	GENIC	heterozygous	50877136
11	30641615	30641616	T	C	64	GENIC	homozygous	50715272
11	30641913	30641914	G	C	30	GENIC	homozygous	50715273