chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	62844960	62844961	C	T	11	GENIC	homozygous	52991786
8	62846629	62846630	A	C	2	GENIC	homozygous	52991787
8	62847303	62847327	CTCCTCTCCTCTCCTCTCCTCTCC	------------------------	4	GENIC	heterozygous	53389600
8	62848930	62848931	G	T	11	GENIC	homozygous	52991793
8	62852000	62852001	T	A	12	GENIC	possibly homozygous	52991794
8	62852132	62852133	A	-	2	GENIC	homozygous	52991795
8	62852560	62852561	A	C	7	GENIC	homozygous	52991796
8	62858115	62858116	G	A	8	GENIC	homozygous	52991799
8	62858280	62858281	G	A	12	GENIC	possibly homozygous	52991800
8	62859209	62859210	T	C	9	GENIC	homozygous	52991801
8	62859785	62859786	C	CCCA	4	GENIC	homozygous	52991804
8	62862107	62862108	G	A	7	GENIC	possibly homozygous	52991807
8	62862403	62862404	G	-	1	GENIC	homozygous	52991808
8	62862795	62862796	A	G	12	GENIC	possibly homozygous	52991809
8	62862834	62862835	T	G	4	GENIC	heterozygous	52991810
8	62862848	62862849	A	G	7	GENIC	possibly homozygous	52991811
8	62863889	62863890	C	T	5	GENIC	heterozygous	52991812
8	62863926	62863927	A	G	7	GENIC	homozygous	52991813
8	62864234	62864235	T	C	7	GENIC	possibly homozygous	52991814
8	62864272	62864273	A	G	2	GENIC	heterozygous	52991815
8	62864615	62864616	C	T	9	GENIC	homozygous	52991816
8	62864918	62864919	T	C	8	GENIC	homozygous	52991820
8	62865028	62865030	AA	--	1	GENIC	homozygous	52991821
8	62865036	62865037	A	C	6	GENIC	heterozygous	53434116
8	62865807	62865808	T	A	11	GENIC	possibly homozygous	52991822
8	62866416	62866417	C	T	15	GENIC	homozygous	52991828
8	62867089	62867090	C	A	3	GENIC	heterozygous	52991829
8	62867146	62867147	G	A	1	GENIC	homozygous	52991830