chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	7818747	7818748	G	A	16	GENIC	homozygous	112483249
4	7819007	7819008	T	C	12	GENIC	homozygous	112483251
4	7819243	7819244	T	C	15	GENIC	homozygous	112483255
4	7819352	7819353	G	C	15	GENIC	homozygous	112483257
4	7819716	7819717	C	T	16	GENIC	homozygous	112483259
4	7819859	7819860	T	C	20	GENIC	homozygous	112483261
4	7819930	7819931	A	G	12	GENIC	homozygous	112483263
4	7819975	7819976	T	C	20	GENIC	homozygous	112483265
4	7820531	7820532	A	G	13	GENIC	homozygous	112483267
4	7820688	7820689	T	C	10	GENIC	homozygous	112483269
4	7820728	7820729	A	G	8	GENIC	homozygous	112483271
4	7820730	7820731	A	G	9	GENIC	homozygous	112483273
4	7820960	7820961	A	T	4	GENIC	homozygous	112483286
4	7821031	7821032	G	A	19	GENIC	homozygous	112483288
4	7821646	7821647	G	A	17	GENIC	homozygous	112483296
4	7821044	7821045	A	C	21	GENIC	homozygous	112483290
4	7821283	7821284	A	G	8	GENIC	homozygous	112483292
4	7821406	7821407	A	G	21	GENIC	homozygous	112483294
4	7821703	7821704	A	G	31	GENIC	homozygous	112483298
4	7822034	7822035	G	A	10	GENIC	homozygous	112483300
4	7822076	7822077	G	A	4	GENIC	homozygous	119272942
4	7822122	7822123	T	C	11	GENIC	homozygous	112483302
4	7822279	7822280	A	G	16	GENIC	homozygous	112483308
4	7822628	7822629	C	G	9	GENIC	homozygous	112483310
4	7822714	7822715	C	G	13	GENIC	heterozygous	112483312