chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	3996029	3996030	G	A	23	GENIC	possibly homozygous	140508267
20	3997668	3997669	T	C	18	GENIC	homozygous	130027243
20	3998236	3998237	G	A	23	GENIC	homozygous	140508268
20	4002222	4002223	A	G	30	GENIC	homozygous	130027246
20	4003716	4003717	T	A	50	GENIC	heterozygous	130027248
20	4003744	4003745	G	T	54	GENIC	heterozygous	130027249
20	4003817	4003818	T	C	52	GENIC	heterozygous	130027250
20	4003835	4003836	C	A	54	GENIC	heterozygous	130027251
20	4003839	4003840	C	T	56	GENIC	heterozygous	140508269
20	4003878	4003879	G	A	56	GENIC	heterozygous	130027252
20	4003894	4003895	G	A	53	GENIC	heterozygous	130027253
20	4003903	4003904	A	C	51	GENIC	heterozygous	130027254
20	4003968	4003969	A	T	33	GENIC	heterozygous	130027255
20	4003986	4003987	A	G	29	GENIC	heterozygous	130027256
20	4004008	4004009	A	G	29	GENIC	heterozygous	130027257
20	4004040	4004041	A	G	15	GENIC	homozygous	140508270
20	4004320	4004321	T	C	50	GENIC	heterozygous	130027263
20	4004335	4004336	G	A	53	GENIC	heterozygous	140508271
20	4004421	4004422	G	A	37	GENIC	heterozygous	140508272
20	4004927	4004928	C	T	28	GENIC	heterozygous	130027265
20	3998670	3998670		AA	26	GENIC	homozygous	140482923
20	4003868	4003868		AT	57	GENIC	heterozygous	129978761
20	4003877	4003877		TG	58	GENIC	heterozygous	129978762
20	4003886	4003888	AC		53	GENIC	heterozygous	129978763
20	4003897	4003899	CA		50	GENIC	heterozygous	129978764
20	4003909	4003913	TGCC		52	GENIC	heterozygous	129978765
20	4003914	4003914		GTAT	51	GENIC	heterozygous	129978766
20	4004033	4004033		TG	23	GENIC	heterozygous	148642086
20	4004087	4004088	A	C	21	GENIC	heterozygous	403460218
20	4004033	4004034	C	T	19	GENIC	heterozygous	404407247
20	4004081	4004082	C	A	21	GENIC	heterozygous	403460216
20	4004082	4004083	A	G	21	GENIC	heterozygous	403460217