chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	30756018	30756019	A	AGGTTT	23	GENIC	homozygous	50715679
11	30756490	30756491	T	A	18	GENIC	homozygous	51103190
11	30756875	30756876	A	ACTT	9	GENIC	homozygous	51103192
11	30757130	30757132	TT	--	5	GENIC	heterozygous	50715686
11	30757131	30757132	T	-	5	GENIC	heterozygous	50877161
11	30757224	30757225	C	T	17	GENIC	homozygous	50916918
11	30757608	30757609	A	T	30	GENIC	homozygous	51103193
11	30757625	30757629	CTGT	----	28	GENIC	homozygous	51103194
11	30757964	30757965	C	CT	6	GENIC	heterozygous	50715687
11	30758330	30758331	C	T	25	GENIC	homozygous	51103195
11	30758600	30758601	G	C	23	GENIC	homozygous	50916921
11	30759034	30759035	C	T	24	GENIC	homozygous	50916922
11	30760656	30760657	A	G	24	GENIC	homozygous	50715689
11	30760802	30760803	A	C	18	GENIC	homozygous	50715690
11	30761198	30761199	G	-	22	GENIC	homozygous	51103196
11	30761845	30761846	G	T	19	GENIC	homozygous	51103197
11	30761912	30761913	T	TG	28	GENIC	homozygous	50715691
11	30762108	30762109	T	A	31	GENIC	homozygous	50916923
11	30762741	30762742	A	G	37	GENIC	homozygous	50715692
11	30763073	30763074	G	T	28	GENIC	homozygous	50715693
11	30764052	30764053	C	T	13	GENIC	homozygous	50916927
11	30765173	30765174	A	C	36	GENIC	homozygous	50715695
11	30765215	30765216	T	C	37	GENIC	homozygous	50916928
11	30765273	30765274	A	G	28	GENIC	homozygous	51103198
11	30765489	30765490	T	C	25	GENIC	possibly homozygous	51103199
11	30766051	30766052	C	A	23	GENIC	homozygous	51103200
11	30766460	30766461	A	G	14	GENIC	homozygous	51103201
11	30766502	30766505	AAT	---	8	GENIC	homozygous	50916929
11	30766819	30766820	C	T	15	GENIC	homozygous	50715697
11	30767328	30767329	A	T	22	GENIC	homozygous	50916931