chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	62859782	62859783	T	TTC	1	GENIC	homozygous	53389605
8	62860156	62860157	G	A	11	GENIC	homozygous	53274486
8	62860708	62860709	C	G	3	GENIC	homozygous	53274487
8	62861677	62861679	CT	--	3	GENIC	homozygous	53461983
8	62861685	62861686	C	T	2	GENIC	homozygous	53461985
8	62862107	62862108	G	A	12	GENIC	homozygous	52991807
8	62862403	62862404	G	-	6	GENIC	heterozygous	52991808
8	62862834	62862835	T	G	10	GENIC	homozygous	52991810
8	62862848	62862849	A	G	4	GENIC	homozygous	52991811
8	62863889	62863890	C	T	10	GENIC	heterozygous	52991812
8	62863926	62863927	A	G	11	GENIC	homozygous	52991813
8	62864012	62864013	G	A	18	GENIC	possibly homozygous	53320437
8	62864234	62864235	T	C	21	GENIC	possibly homozygous	52991814
8	62864272	62864273	A	G	8	GENIC	heterozygous	52991815
8	62864852	62864853	A	G	4	GENIC	heterozygous	53320438
8	62864918	62864919	T	C	15	GENIC	possibly homozygous	52991820
8	62865028	62865030	AA	--	4	GENIC	heterozygous	52991821
8	62865807	62865808	T	A	13	GENIC	homozygous	52991822
8	62865979	62865980	G	GT	1	GENIC	homozygous	52991823
8	62866416	62866417	C	T	15	GENIC	possibly homozygous	52991828
8	62867089	62867090	C	A	3	GENIC	homozygous	52991829
8	62867146	62867147	G	A	1	GENIC	homozygous	52991830