chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	11789791	11789792	A	G	22	GENIC	homozygous	116734453
10	11789878	11789879	G	T	18	GENIC	homozygous	116495425
10	11790216	11790220	TATT		34	GENIC	homozygous	128790073
10	11790322	11790323	G	A	18	GENIC	homozygous	116495427
10	11790912	11790913	T		7	GENIC	homozygous	128790074
10	11791749	11791751	AC		23	GENIC	homozygous	128790075
10	11792512	11792513	A	C	30	GENIC	homozygous	116495429
10	11793422	11793423	G	A	29	GENIC	homozygous	116495431
10	11794061	11794062	C	T	18	GENIC	homozygous	117120230
10	11797216	11797217	A	G	16	GENIC	homozygous	116495437
10	11794079	11794080	T	A	19	GENIC	homozygous	117215751
10	11794658	11794659	A	G	29	GENIC	homozygous	116495433
10	11796837	11796838	T	G	16	GENIC	homozygous	116495435
10	11800928	11800929	C	T	23	GENIC	homozygous	116495439
10	11802035	11802036	A	G	18	GENIC	homozygous	116495441
10	11802272	11802273	A	G	22	GENIC	homozygous	116495443
10	11804124	11804125	A	G	21	GENIC	homozygous	116495445
10	11805172	11805174	TG		15	GENIC	homozygous	128790076
10	11805469	11805469		TGTGCATGCACATGCACATGCACA	21	GENIC	homozygous	128790077