chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	59531815	59531816	C	T	11	GENIC	homozygous	117079609
10	59532947	59532948	G	T	14	GENIC	homozygous	117079610
10	59534738	59534739	G	A	22	GENIC	homozygous	116788582
10	59535290	59535291	T	C	9	GENIC	homozygous	116788586
10	59535777	59535778	A	T	31	GENIC	homozygous	116937664
10	59536922	59536923	G	A	18	GENIC	homozygous	117079612
10	59537129	59537130	G	A	13	GENIC	homozygous	117079614
10	59537688	59537689	T	C	20	GENIC	homozygous	117079615
10	59537758	59537759	T	G	9	GENIC	homozygous	116788590
10	59538782	59538783	C	G	24	GENIC	homozygous	117079617
10	59542174	59542175	G	A	12	GENIC	homozygous	117079618
10	59538839	59538840	C	A	20	GENIC	homozygous	116608217
10	59545505	59545506	T	C	23	GENIC	homozygous	116608241
10	59549501	59549502	G	A	23	GENIC	homozygous	117079620
10	59550147	59550148	A	C	12	GENIC	homozygous	116608253
10	59550465	59550466	G	A	9	GENIC	homozygous	117079621
10	59550935	59550936	T	A	16	GENIC	homozygous	117079623
10	59552185	59552186	C	T	21	GENIC	homozygous	117079625
10	59552286	59552287	G	A	26	GENIC	homozygous	117079626
10	59552341	59552342	C	G	9	GENIC	heterozygous	117079628
10	59552492	59552493	G	A	7	GENIC	heterozygous	126431486
10	59554080	59554081	T	G	9	GENIC	heterozygous	116608267
10	59557050	59557051	A	G	16	GENIC	homozygous	116608273
10	59558325	59558326	A	G	9	GENIC	homozygous	116608279