chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	47755116	47755117	C	G	39	GENIC	homozygous	51446410
10	47756471	47756472	T	C	24	GENIC	homozygous	51446413
10	47757723	47757724	A	G	44	GENIC	homozygous	51446414
10	47759218	47759219	A	G	42	GENIC	possibly homozygous	52054568
10	47759784	47759785	G	A	22	GENIC	homozygous	52054570
10	47760367	47760368	T	-	13	GENIC	heterozygous	51877359
10	47761615	47761616	T	G	44	GENIC	homozygous	51446418
10	47762345	47762346	G	GTTT	26	GENIC	possibly homozygous	51638447
10	47761337	47761338	T	TG	17	GENIC	possibly homozygous	51638446
10	47762353	47762354	T	TTTTG	26	GENIC	heterozygous	51638448
10	47762353	47762354	T	TTTG	26	GENIC	possibly homozygous	52054572
10	47764065	47764066	T	C	43	GENIC	homozygous	52054574
10	47768503	47768504	A	AC	35	GENIC	homozygous	51446421
10	47768617	47768618	A	G	38	GENIC	homozygous	51446422
10	47770254	47770255	T	C	22	GENIC	homozygous	51446423
10	47772851	47772852	G	C	21	GENIC	homozygous	52054576