chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	34672840	34672841	T	C	9	GENIC	homozygous	118128301
10	34672848	34672849	T	C	10	GENIC	homozygous	118128302
10	34672890	34672891	G	A	13	GENIC	homozygous	118128303
10	34672899	34672900	T	C	14	GENIC	homozygous	118128304
10	34672987	34672988	A	C	36	GENIC	homozygous	118128305
10	34673022	34673023	C	T	24	GENIC	homozygous	118128306
10	34673028	34673029	T	G	20	GENIC	homozygous	118128307
10	34673088	34673089	T	C	6	GENIC	homozygous	118128308
10	34673112	34673113	A	T	8	GENIC	homozygous	118128309
10	34673250	34673251	T	C	37	GENIC	homozygous	118065316
10	34673313	34673314	T	C	32	GENIC	homozygous	118065317
10	34673349	34673350	C	T	24	GENIC	heterozygous	118128310
10	34673419	34673420	G	A	13	GENIC	heterozygous	118128311
10	34673464	34673465	A	G	3	GENIC	homozygous	116756939
10	34673517	34673518	G	T	10	GENIC	homozygous	118128312
10	34673526	34673527	G	A	11	GENIC	homozygous	118128313
10	34673565	34673566	C	T	12	GENIC	homozygous	118128314
10	34673625	34673626	A	G	10	GENIC	homozygous	118128315
10	34673640	34673641	T	G	10	GENIC	homozygous	118128316