chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	8272651	8272652	C	G	17	GENIC	possibly homozygous	45416637
20	8273126	8273127	C	G	22	GENIC	possibly homozygous	45863007
20	8273513	8273514	A	C	24	GENIC	homozygous	45416645
20	8274677	8274678	A	G	20	GENIC	possibly homozygous	45863008
20	8274854	8274855	G	A	20	GENIC	homozygous	45863009
20	8275519	8275520	C	G	14	GENIC	possibly homozygous	45863011
20	8275741	8275743	GT	--	13	GENIC	possibly homozygous	45863012
20	8275850	8275851	T	A	16	GENIC	possibly homozygous	45863013
20	8276793	8276794	C	T	5	GENIC	heterozygous	45863015
20	8276909	8276910	C	T	14	GENIC	homozygous	45863016
20	8276982	8276983	T	C	10	GENIC	heterozygous	45416666
20	8277289	8277290	T	C	28	GENIC	possibly homozygous	45863017
20	8278331	8278332	C	T	21	GENIC	homozygous	45863021
20	8278844	8278845	T	A	20	GENIC	possibly homozygous	45416677
20	8279165	8279166	G	T	6	GENIC	homozygous	45863022
20	8279184	8279185	T	G	3	GENIC	heterozygous	45863023
20	8279190	8279192	TT	--	4	GENIC	heterozygous	45863024
20	8279203	8279204	T	TTG	4	GENIC	heterozygous	45863025
20	8279269	8279270	A	C	10	GENIC	homozygous	45863026
20	8279595	8279596	G	A	10	GENIC	possibly homozygous	45863027
20	8279599	8279600	G	C	8	GENIC	possibly homozygous	45416683
20	8279818	8279819	G	A	16	GENIC	homozygous	45863028
20	8280488	8280489	C	T	20	GENIC	possibly homozygous	45863029
20	8280524	8280525	T	C	18	GENIC	homozygous	45416685
20	8280670	8280671	C	G	15	GENIC	homozygous	45863030
20	8280787	8280788	G	A	8	GENIC	possibly homozygous	45863031
20	8280788	8280789	G	T	7	GENIC	possibly homozygous	45863032
20	8280826	8280827	G	T	7	GENIC	homozygous	45863033
20	8280834	8280835	A	-	5	GENIC	homozygous	45863034
20	8280894	8280895	G	T	6	GENIC	homozygous	45863035
20	8280929	8280930	T	G	3	GENIC	homozygous	45863036
20	8280971	8280972	C	CTTTTT	2	GENIC	homozygous	45863037
20	8280992	8280993	G	A	2	GENIC	homozygous	45863038