chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	10132353	10132354	A	G	35	GENIC	homozygous	45425627
20	10132355	10132356	A	G	35	GENIC	homozygous	45425628
20	10132670	10132671	T	C	28	GENIC	homozygous	45425629
20	10132721	10132722	A	T	24	GENIC	homozygous	45425630
20	10132953	10132954	G	GCCTTCC	21	GENIC	homozygous	45425631
20	10133188	10133189	G	A	34	GENIC	homozygous	45738409
20	10135366	10135367	G	A	41	GENIC	homozygous	45738410
20	10135493	10135494	G	C	31	GENIC	homozygous	45738411
20	10135533	10135538	GGGGG	-----	22	GENIC	possibly homozygous	45738412
20	10136255	10136258	AAA	---	23	GENIC	homozygous	45756610
20	10136472	10136473	G	A	35	GENIC	homozygous	45738413
20	10136825	10136826	G	A	24	GENIC	homozygous	45738414
20	10136864	10136865	T	C	27	GENIC	homozygous	45425637
20	10136888	10136889	A	T	24	GENIC	homozygous	45738415
20	10136974	10136975	C	CTT	10	GENIC	heterozygous	45425638
20	10137473	10137474	T	TC	11	GENIC	heterozygous	45425641
20	10140080	10140081	C	CATCTATCTATCT	4	GENIC	homozygous	45962429
20	10140485	10140486	A	G	24	GENIC	homozygous	45425648