chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	30756018	30756019	A	AGGTTT	31	GENIC	homozygous	50715679
11	30756289	30756290	C	CA	33	GENIC	homozygous	50715680
11	30756563	30756564	G	-	15	GENIC	heterozygous	50715681
11	30756564	30756566	GA	--	16	GENIC	heterozygous	50715682
11	30757128	30757132	TTTT	----	24	GENIC	homozygous	50715685
11	30757964	30757965	C	CT	12	GENIC	heterozygous	50715687
11	30757965	30757966	T	-	12	GENIC	heterozygous	50715688
11	30760656	30760657	A	G	22	GENIC	homozygous	50715689
11	30760802	30760803	A	C	22	GENIC	homozygous	50715690
11	30761912	30761913	T	TG	30	GENIC	homozygous	50715691
11	30762741	30762742	A	G	26	GENIC	homozygous	50715692
11	30763073	30763074	G	T	39	GENIC	homozygous	50715693
11	30763912	30763913	T	TA	21	GENIC	possibly homozygous	50715694
11	30765173	30765174	A	C	36	GENIC	homozygous	50715695
11	30766480	30766481	A	AAAATAAATAAATAAAT	1	GENIC	homozygous	51275151
11	30766663	30766664	G	A	8	GENIC	homozygous	50715696
11	30766819	30766820	C	T	17	GENIC	homozygous	50715697