chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	74370684	74370685	T	C	18	GENIC	possibly homozygous	111614566
3	74370699	74370700	T	A	27	GENIC	possibly homozygous	111614568
3	74370765	74370766	A	G	40	GENIC	homozygous	111614570
3	74370779	74370780	C	A	34	GENIC	homozygous	111614572
3	74370780	74370781	T	A	36	GENIC	homozygous	111614574
3	74370804	74370805	C	T	34	GENIC	possibly homozygous	111614576
3	74370852	74370853	G	A	41	GENIC	heterozygous	111614578
3	74371301	74371302	C	A	34	GENIC	homozygous	111614580
3	74371498	74371499	G	T	51	GENIC	homozygous	111614582
3	74372049	74372050	C	T	45	GENIC	homozygous	111614583
3	74372691	74372692	A	G	8	GENIC	homozygous	111614585
3	74372824	74372825	T	A	23	GENIC	homozygous	111614587
3	74373207	74373208	T	C	19	GENIC	homozygous	111614589
3	74373869	74373870	C	A	43	GENIC	homozygous	111614591
3	74374803	74374804	C	T	5	GENIC	homozygous	111614593