chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	88120994	88120995	C	T	37	GENIC	homozygous	53163277
10	88121835	88121837	TT	--	14	GENIC	homozygous	52507606
10	88122090	88122091	C	CCCACCCCCCCCTTTTTAATTAAAGCTCT	22	GENIC	heterozygous	52462140
10	88122270	88122271	A	ATTT	9	GENIC	homozygous	52393612
10	88123107	88123108	A	G	29	GENIC	homozygous	52205815
10	88123123	88123124	C	T	29	GENIC	homozygous	53163279
10	88123377	88123378	C	G	24	GENIC	homozygous	52205823
10	88123656	88123657	A	AAAAG	7	GENIC	homozygous	53163281
10	88126423	88126428	TTTTT	-----	25	GENIC	homozygous	53163283
10	88126427	88126428	T	TGG	23	GENIC	homozygous	53163285
10	88126484	88126485	C	T	29	GENIC	homozygous	53163287
10	88126600	88126601	T	C	25	GENIC	homozygous	53163289
10	88126645	88126646	A	AGTGTGT	21	GENIC	homozygous	52322831
10	88126692	88126693	A	ATGTG	28	GENIC	possibly homozygous	52462141
10	88126747	88126751	TGTG	----	34	GENIC	homozygous	53163291
10	88126879	88126885	TGTGTG	------	11	GENIC	homozygous	53163293
10	88128019	88128020	A	T	29	GENIC	homozygous	52205853