chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	82249487	82249488	C	T	41	GENIC	homozygous	116658245
10	82249556	82249557	T	G	32	GENIC	homozygous	116658247
10	82250290	82250291	A	C	53	GENIC	homozygous	116658249
10	82250536	82250537	A	G	48	GENIC	homozygous	116658251
10	82251202	82251203	G	A	34	GENIC	homozygous	116980495
10	82252731	82252732	C	G	24	GENIC	possibly homozygous	116658253
10	82252763	82252764	G	A	28	GENIC	homozygous	116658255
10	82252779	82252780	C	A	39	GENIC	homozygous	116658257
10	82252828	82252829	A	G	37	GENIC	homozygous	116658259
10	82253519	82253520	A	G	59	GENIC	homozygous	116658261
10	82253547	82253548	T	A	51	GENIC	homozygous	116658263
10	82253618	82253619	T	C	34	GENIC	homozygous	116658265
10	82255445	82255446	C	T	42	GENIC	homozygous	116658269
10	82255977	82255978	T	C	17	GENIC	possibly homozygous	118003474
10	82256125	82256126	T	C	21	GENIC	possibly homozygous	118003475
10	82256301	82256302	A	G	56	GENIC	homozygous	116658271