chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	70790983	70790984	C	T	16	GENIC	homozygous	116628454
10	70791123	70791124	G	A	15	GENIC	homozygous	116628456
10	70791329	70791330	G	A	11	GENIC	homozygous	116628458
10	70791451	70791452	C	T	9	GENIC	homozygous	116628460
10	70792512	70792513	G	A	12	GENIC	homozygous	116628462
10	70792568	70792569	G	C	13	GENIC	homozygous	116628464
10	70793630	70793631	T	C	8	GENIC	homozygous	116628466
10	70793665	70793666	A	G	22	GENIC	homozygous	116628468
10	70793739	70793740	T	C	11	GENIC	homozygous	117130980
10	70793959	70793960	G	A	18	GENIC	homozygous	116628470
10	70794316	70794317	T	C	17	GENIC	homozygous	116628472
10	70794465	70794466	G	A	20	GENIC	homozygous	117222682
10	70794551	70794552	A	G	17	GENIC	homozygous	116628474
10	70794729	70794730	G	A	8	GENIC	homozygous	117222684
10	70795134	70795135	A	C	22	GENIC	homozygous	116628476
10	70795406	70795407	G	C	4	GENIC	heterozygous	126422838
10	70795408	70795409	G	C	4	GENIC	heterozygous	117222686
10	70795413	70795414	C	G	3	GENIC	heterozygous	117344863
10	70796182	70796183	C	T	19	GENIC	homozygous	116628478
10	70796377	70796378	A	C	5	GENIC	homozygous	116628480
10	70796603	70796604	G	A	9	GENIC	homozygous	116628482
10	70796886	70796887	G	T	6	GENIC	heterozygous	118000376
10	70797195	70797196	C	T	22	GENIC	possibly homozygous	116628486
10	70798534	70798535	C	T	11	GENIC	homozygous	118000377
10	70799091	70799092	T	C	15	GENIC	homozygous	116628488
10	70799684	70799685	C	T	4	GENIC	homozygous	116628490
10	70799686	70799687	G	A	5	GENIC	homozygous	116628492
10	70800187	70800188	G	C	24	GENIC	homozygous	116799387
10	70800366	70800367	G	T	17	GENIC	homozygous	116628494
10	70801189	70801190	G	A	17	GENIC	homozygous	116628496