chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	24920616	24920617	A	T	6	GENIC	homozygous	110812143
18	24921046	24921047	G	A	23	GENIC	homozygous	110309500
18	24921303	24921304	G	A	38	GENIC	homozygous	110309502
18	24922763	24922764	T	A	37	GENIC	homozygous	110309504
18	24923219	24923220	T	G	38	GENIC	homozygous	110309506
18	24924069	24924070	T	G	22	GENIC	homozygous	110309508
18	24925008	24925009	C	T	36	GENIC	homozygous	110309510
18	24925414	24925415	A	G	38	GENIC	homozygous	110309512
18	24925721	24925722	A	G	34	GENIC	homozygous	110309514
18	24925903	24925904	T	G	36	GENIC	homozygous	110309516
18	24926079	24926080	C	T	32	GENIC	homozygous	110309518
18	24926133	24926134	C	T	31	GENIC	homozygous	110309520
18	24926164	24926165	T	C	34	GENIC	homozygous	110309522
18	24926211	24926212	G	A	30	GENIC	homozygous	110309524
18	24926446	24926447	C	T	26	GENIC	homozygous	110309526
18	24926767	24926768	A	G	24	GENIC	homozygous	110309528
18	24927406	24927407	G	A	21	GENIC	homozygous	110309531
18	24927427	24927428	G	A	23	GENIC	homozygous	110309533
18	24927498	24927499	A	G	37	GENIC	homozygous	110309535
18	24927865	24927866	T	C	26	GENIC	homozygous	110309538
18	24928130	24928131	A	G	24	GENIC	homozygous	110309540