chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	41646569	41646570	A	AT	10	GENIC	heterozygous	52598859
8	41649672	41649673	T	C	13	GENIC	heterozygous	52598918
8	41650813	41650814	A	AT	19	GENIC	heterozygous	52599008
8	41651149	41651150	A	AG	6	GENIC	heterozygous	52599019
8	41651150	41651151	G	-	6	GENIC	heterozygous	52599024
8	41651223	41651224	A	AG	5	GENIC	heterozygous	52599029
8	41651223	41651224	A	AC	5	GENIC	heterozygous	52599031
8	41651281	41651282	C	CA	3	GENIC	heterozygous	52599037
8	41651284	41651285	A	AG	5	GENIC	heterozygous	52599043
8	41651368	41651369	A	AG	5	GENIC	heterozygous	52599046
8	41651387	41651388	A	T	2	GENIC	homozygous	52599048
8	41651446	41651447	G	GT	13	GENIC	heterozygous	52599054
8	41652819	41652820	G	GT	51	GENIC	heterozygous	52599112
8	41653863	41653867	AGAG	----	29	GENIC	heterozygous	52599213
8	41657078	41657079	C	CCTCCCCG	2	GENIC	heterozygous	53379022
8	41657218	41657219	A	-	20	GENIC	heterozygous	52599388
8	41657221	41657222	C	-	20	GENIC	heterozygous	52599391
8	41657707	41657708	G	GT	1	GENIC	homozygous	53363285
8	41658461	41658462	A	-	8	GENIC	heterozygous	53363286
8	41658733	41658734	G	T	4	GENIC	heterozygous	52599421
8	41660620	41660621	G	T	13	GENIC	heterozygous	52599482
8	41661270	41661271	A	-	20	GENIC	heterozygous	52599524
8	41662424	41662425	C	-	3	GENIC	heterozygous	52965666