chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	49889353	49889354	G	GGTGTGTGTGTGTGTGTGT	21	GENIC	homozygous	50513821
12	49890647	49890648	A	ACC	2	GENIC	homozygous	50513823
12	49890689	49890690	A	AC	3	GENIC	heterozygous	50235075
12	49891718	49891730	ACACACACACAC	------------	14	GENIC	heterozygous	50546756
12	49891720	49891730	ACACACACAC	----------	14	GENIC	heterozygous	50546757
12	49891952	49891953	T	C	53	GENIC	homozygous	50235079
12	49892515	49892516	A	G	33	GENIC	homozygous	50235081
12	49892564	49892565	C	CG	40	GENIC	homozygous	50235083
12	49892994	49892995	A	G	38	GENIC	homozygous	50235085
12	49893006	49893007	C	T	37	GENIC	homozygous	50235087
12	49893666	49893667	G	A	36	GENIC	homozygous	50235089
12	49895907	49895908	A	C	26	GENIC	homozygous	50235091
12	49897028	49897029	G	T	35	GENIC	homozygous	50235093
12	49897105	49897106	G	C	37	GENIC	homozygous	50235095
12	49899043	49899044	T	C	40	GENIC	homozygous	50235097
12	49899940	49899941	A	AATAGGTAAGGGGTAGCTAGAAATGGGGACACTGAGACTGGTCAGGTCACACAGGTT	50	GENIC	homozygous	50546758
12	49900592	49900593	C	T	34	GENIC	homozygous	50235099
12	49900691	49900692	G	A	48	GENIC	homozygous	50235101
12	49902577	49902578	G	A	17	GENIC	homozygous	50235103
12	49903130	49903131	C	A	71	GENIC	homozygous	50235105
12	49903419	49903420	A	AATGCACACACATACAC	3	GENIC	homozygous	50546759
12	49903481	49903482	C	CGCATGCACACACATAA	44	GENIC	homozygous	50546760
12	49904879	49904883	AAAA	----	12	GENIC	homozygous	50235119
12	49904882	49904883	A	ACC	11	GENIC	homozygous	50546761
12	49905167	49905168	G	A	30	GENIC	homozygous	50235121
12	49907140	49907141	A	T	25	GENIC	homozygous	50235123