chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	97269973	97269974	G	A	13	GENIC	homozygous	53170366
10	97269983	97269984	C	T	7	GENIC	homozygous	53170368
10	97270468	97270469	A	G	12	GENIC	homozygous	53170370
10	97270625	97270626	G	A	7	GENIC	possibly homozygous	53170372
10	97270803	97270804	A	G	12	GENIC	homozygous	53170374
10	97271401	97271404	ACC	---	3	GENIC	heterozygous	53170376
10	97271407	97271416	CCAGGTACC	---------	2	GENIC	heterozygous	53170378
10	97271507	97271508	A	G	18	GENIC	homozygous	53170380
10	97271534	97271535	G	A	17	GENIC	possibly homozygous	53170382
10	97271573	97271574	C	T	12	GENIC	homozygous	53170384
10	97271738	97271739	A	G	10	GENIC	homozygous	53170386
10	97271958	97271959	A	G	13	GENIC	homozygous	53170388
10	97272340	97272341	G	A	14	GENIC	homozygous	53170390