chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	30711617	30711618	A	G	57	GENIC	homozygous	120187984
2	30711698	30711699	C	G	62	GENIC	homozygous	111098525
2	30711801	30711802	C	T	52	GENIC	homozygous	111098527
2	30715210	30715211	G	A	51	GENIC	homozygous	110501594
2	30716124	30716126	GA		32	GENIC	homozygous	132560246
2	30716438	30716455	GGGTGATGGTGTCTTGG		34	GENIC	possibly homozygous	131289629
2	30718573	30718574	G	T	60	GENIC	possibly homozygous	120187985
2	30718613	30718614	A	G	55	GENIC	homozygous	110501598
2	30719093	30719094	A	G	43	GENIC	homozygous	111233321
2	30719507	30719508	A	C	50	GENIC	homozygous	110501602
2	30719609	30719610	T	C	35	GENIC	homozygous	110501604
2	30720543	30720544	A	G	34	GENIC	homozygous	110501606
2	30720969	30720970	A	G	63	GENIC	homozygous	111233325
2	30721231	30721231		TCT	65	GENIC	homozygous	130244121
2	30722113	30722114	T	C	18	GENIC	homozygous	110501612
2	30722817	30722818	A	T	51	GENIC	homozygous	111233335
2	30724251	30724252	C	T	58	GENIC	homozygous	110501618
2	30724381	30724382	C	G	53	GENIC	homozygous	110501620
2	30724410	30724411	C	T	51	GENIC	homozygous	110501622
2	30724473	30724474	A	T	37	GENIC	homozygous	110501624
2	30724482	30724483	T	A	36	GENIC	homozygous	110501626
2	30724514	30724515	A		37	GENIC	homozygous	130244123
2	30724833	30724834	C	T	55	GENIC	homozygous	110501628
2	30732313	30732317	TGGT		48	GENIC	homozygous	131289633
2	30732833	30732834	T		48	GENIC	homozygous	133075118
2	30733618	30733619	A	G	59	GENIC	homozygous	110501656
2	30734724	30734725	G	C	57	GENIC	homozygous	110501660
2	30735389	30735390	A	G	57	GENIC	homozygous	111233357
2	30735423	30735424	A	G	58	GENIC	homozygous	111233359