chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	60282180	60282181	G	A	59	GENIC	homozygous	142251973
10	60282768	60282769	G	C	54	GENIC	homozygous	138801223
10	60283573	60283573		AAAC	36	GENIC	homozygous	142204382
10	60283904	60283905	A	G	37	GENIC	homozygous	142251974
10	60284501	60284502	A		43	GENIC	homozygous	142204383
10	60284508	60284509	A	C	46	GENIC	homozygous	142251975
10	60284640	60284641	T	C	44	GENIC	homozygous	142251976
10	60285042	60285043	G	A	49	GENIC	homozygous	142251977
10	60285747	60285748	C	T	58	GENIC	homozygous	142251978
10	60286809	60286810	T	C	53	GENIC	homozygous	142251979
10	60286832	60286833	G	A	51	GENIC	homozygous	138801225
10	60288241	60288242	G	T	30	GENIC	homozygous	142251980
10	60288633	60288634	A	T	33	GENIC	homozygous	138801226
10	60290463	60290464	G	A	49	GENIC	homozygous	138801227
10	60292360	60292361	T	G	48	GENIC	homozygous	138801231
10	60293250	60293251	T	C	60	GENIC	homozygous	138801233
10	60294986	60294987	G	A	68	GENIC	homozygous	138801234
10	60295307	60295308	G	A	68	GENIC	homozygous	138801235