chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	21486665	21486666	T	-	57	GENIC	heterozygous	50110696
12	21487280	21487281	C	CAA	61	GENIC	heterozygous	50537780
12	21487283	21487285	GT	--	75	GENIC	heterozygous	50537782
12	21487656	21487657	A	T	42	GENIC	heterozygous	50110721
12	21488470	21488471	T	TTTGGAAAGTTC	40	GENIC	heterozygous	50537788
12	21488499	21488500	A	AT	46	GENIC	heterozygous	50110751
12	21488669	21488673	GCCC	----	15	GENIC	heterozygous	50537790
12	21488675	21488676	T	TTGGA	14	GENIC	heterozygous	50537792
12	21490458	21490459	A	-	3	GENIC	homozygous	50110761
12	21491208	21491209	A	ACACG	7	GENIC	possibly homozygous	50110763
12	21491906	21491907	A	C	21	GENIC	homozygous	50110765
12	21493234	21493235	G	A	25	GENIC	homozygous	50110767
12	21494276	21494277	A	-	11	GENIC	homozygous	50110800
12	21494292	21494293	C	T	9	GENIC	homozygous	50110802
12	21495952	21495953	C	CAA	4	GENIC	homozygous	50110820
12	21495981	21495982	T	TG	11	GENIC	homozygous	50110822
12	21495990	21495991	T	C	15	GENIC	homozygous	50110824
12	21496003	21496004	T	C	23	GENIC	homozygous	50110826
12	21496008	21496009	T	G	28	GENIC	homozygous	50110828
12	21496068	21496069	G	A	8	GENIC	homozygous	50110830
12	21496318	21496319	G	A	11	GENIC	homozygous	50110832
12	21496876	21496877	G	GT	7	GENIC	heterozygous	50110834
12	21496876	21496877	G	GTT	7	GENIC	heterozygous	50557514
12	21497155	21497156	C	CTGTGTGTGTG	1	GENIC	homozygous	50537797
12	21507629	21507630	T	-	17	GENIC	possibly homozygous	50110846
12	21508194	21508195	T	TTCCCCTCACAGATAGAATAACACAGTACAGATTGATCAA	13	GENIC	homozygous	50537799
12	21508199	21508200	C	CAAATGTCA	16	GENIC	heterozygous	50537803
12	21508201	21508202	T	-	16	GENIC	heterozygous	50537805
12	21508224	21508225	C	-	29	GENIC	heterozygous	50110850
12	21508361	21508362	C	CA	77	GENIC	heterozygous	50110864
12	21508399	21508400	T	-	77	GENIC	heterozygous	50110868