chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	30633306	30633307	T	C	18	GENIC	homozygous	50715246
11	30633698	30633699	A	C	10	GENIC	homozygous	50715247
11	30634214	30634215	T	C	13	GENIC	homozygous	50715249
11	30634652	30634653	A	G	19	GENIC	homozygous	50715250
11	30634972	30634973	T	C	25	GENIC	homozygous	50715251
11	30635592	30635593	C	T	22	GENIC	homozygous	50715252
11	30635941	30635942	A	C	19	GENIC	homozygous	50715253
11	30636407	30636408	G	A	24	GENIC	possibly homozygous	50916807
11	30636551	30636552	A	AAATTTTCTCT	14	GENIC	homozygous	50715254
11	30636710	30636711	T	TCA	21	GENIC	homozygous	50715255
11	30637045	30637046	G	A	19	GENIC	homozygous	50715256
11	30637641	30637642	A	G	21	GENIC	homozygous	50715257
11	30637964	30637965	C	T	15	GENIC	homozygous	50715258
11	30638108	30638109	G	A	22	GENIC	homozygous	50715259
11	30638596	30638597	A	G	15	GENIC	homozygous	50715260
11	30639139	30639140	A	G	18	GENIC	homozygous	50715263
11	30640099	30640100	A	G	8	GENIC	homozygous	50715264
11	30640558	30640559	G	A	22	GENIC	homozygous	50715265
11	30640681	30640682	A	ATAATAATAATAATAAT	13	GENIC	homozygous	51178433
11	30640791	30640792	C	G	9	GENIC	homozygous	50715267
11	30641615	30641616	T	C	10	GENIC	homozygous	50715272
11	30641913	30641914	G	C	12	GENIC	homozygous	50715273