chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	35170148	35170149	T	C	21	GENIC	possibly homozygous	50728763
11	35170797	35170798	G	-	3	GENIC	heterozygous	50728769
11	35170921	35170922	G	C	17	GENIC	homozygous	50923674
11	35172192	35172193	T	C	19	GENIC	possibly homozygous	50728776
11	35175403	35175404	C	T	8	GENIC	possibly homozygous	50923677
11	35176252	35176253	G	A	31	GENIC	possibly homozygous	50923680
11	35177078	35177079	A	G	7	GENIC	heterozygous	50923683
11	35177105	35177106	G	A	5	GENIC	homozygous	50923686
11	35177220	35177221	G	T	12	GENIC	homozygous	51400172
11	35177262	35177263	G	A	15	GENIC	heterozygous	50923691
11	35177334	35177335	A	G	10	GENIC	homozygous	50728782
11	35178648	35178649	T	C	9	GENIC	homozygous	50923705
11	35178754	35178755	A	ATGGGACAATTGTTTTTTTTTTTTGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAGCCC	11	GENIC	possibly homozygous	51159778
11	35179775	35179776	T	C	19	GENIC	homozygous	50728786
11	35179868	35179869	C	T	19	GENIC	homozygous	50923728
11	35180225	35180226	T	C	22	GENIC	homozygous	50923730
11	35180559	35180560	T	C	12	GENIC	homozygous	50923733
11	35181354	35181355	C	T	17	GENIC	heterozygous	50923735
11	35181355	35181356	A	G	17	GENIC	heterozygous	50923737
11	35182968	35182969	T	A	4	GENIC	heterozygous	50923755
11	35183863	35183864	C	T	6	GENIC	heterozygous	50923758
11	35183867	35183868	T	-	6	GENIC	homozygous	50728794
11	35184469	35184470	G	A	21	GENIC	possibly homozygous	51400180
11	35185755	35185756	G	A	22	GENIC	homozygous	50728797
11	35186120	35186121	A	T	15	GENIC	homozygous	50728798
11	35186133	35186134	T	A	4	GENIC	homozygous	50728799
11	35186134	35186135	A	G	4	GENIC	homozygous	50728800
11	35186171	35186172	C	T	10	GENIC	homozygous	50728801