chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	90296364	90296365	A	G	39	GENIC	homozygous	116676026
10	90296478	90296478		C	19	GENIC	possibly homozygous	128844124
10	90296579	90296582	TAA		24	GENIC	heterozygous	132147128
10	90299354	90299355	G	A	31	GENIC	homozygous	116676028
10	90299845	90299858	GGATCTCCGAGTG		63	GENIC	homozygous	128844125
10	90298960	90298961	G	A	47	GENIC	homozygous	116904511
10	90300297	90300298	G	A	39	GENIC	homozygous	116904513
10	90300301	90300301		TTCTC	38	GENIC	homozygous	128844126
10	90301669	90301670	A	G	57	GENIC	possibly homozygous	116676030
10	90302063	90302064	T	C	48	GENIC	homozygous	116676032
10	90302501	90302502	T	C	46	GENIC	homozygous	117068525
10	90304992	90304992		G	34	GENIC	homozygous	128844127
10	90305307	90305308	G	A	70	GENIC	homozygous	116676034
10	90305927	90305928	C	A	51	GENIC	homozygous	116676036
10	90307215	90307216	A	G	45	GENIC	homozygous	116904515
10	90309084	90309085	G	A	68	GENIC	homozygous	116904517
10	90309601	90309602	T	C	57	GENIC	homozygous	116676040
10	90309929	90309930	A	G	29	GENIC	homozygous	118007697