chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	7521390	7521391	T		12	GENIC	homozygous	129655786
20	7521391	7521392	A	G	12	GENIC	homozygous	109542469
20	7521395	7521395		G	12	GENIC	homozygous	129655787
20	7521396	7521397	C	G	13	GENIC	homozygous	109542471
20	7521399	7521400	T	C	14	GENIC	homozygous	109542473
20	7521401	7521402	A	G	13	GENIC	homozygous	109542475
20	7521407	7521408	A	G	14	GENIC	homozygous	124631706
20	7521423	7521432	AAAACCCTT		9	GENIC	homozygous	129655788
20	7521435	7521439	TCTA		9	GENIC	homozygous	129655789
20	7521459	7521459		T	8	GENIC	homozygous	129655790
20	7521472	7521472		GTGG	8	GENIC	homozygous	129655791
20	7521475	7521475		GC	9	GENIC	homozygous	129655792
20	7521478	7521478		GGG	9	GENIC	homozygous	129655793
20	7521480	7521480		ACCCACT	9	GENIC	homozygous	129655794
20	7521481	7521482	A	C	9	GENIC	homozygous	129708248
20	7521461	7521462	A	G	8	GENIC	homozygous	129708244
20	7521466	7521467	A	G	9	GENIC	homozygous	129708245
20	7521472	7521473	A	G	9	GENIC	homozygous	129708246
20	7521476	7521477	T	G	9	GENIC	homozygous	129708247
20	7521485	7521485		TTC	9	GENIC	homozygous	129655795
20	7521488	7521489	A	T	10	GENIC	homozygous	129708249
20	7521490	7521490		GTCTTT	10	GENIC	homozygous	129655796
20	7521491	7521492	T	C	11	GENIC	homozygous	129708250
20	7521498	7521498		TTTC	12	GENIC	homozygous	129655797
20	7521536	7521537	T		10	GENIC	homozygous	129655798
20	7521541	7521542	A		10	GENIC	homozygous	129655799
20	7574475	7574505	CTCATAATGTCATAACCGTGGTGTGTGTGT		12	GENIC	heterozygous	130490078
20	7568717	7568719	AT		9	GENIC	heterozygous	130801406