chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	24206010	24206011	T	C	21	GENIC	homozygous	110999397
17	24206022	24206023	C	T	20	GENIC	homozygous	110999399
17	24206852	24206853	T	C	28	GENIC	homozygous	110999401
17	24206995	24206996	T	C	32	GENIC	homozygous	110999403
17	24207270	24207271	T	C	15	GENIC	homozygous	110999405
17	24207363	24207364	C	T	30	GENIC	homozygous	110999407
17	24208224	24208225	C	T	34	GENIC	homozygous	110999409
17	24208251	24208252	G	A	33	GENIC	possibly homozygous	110999411
17	24208592	24208593	A	G	11	GENIC	homozygous	111180591
17	24208784	24208785	A	C	13	GENIC	homozygous	110999413
17	24209147	24209148	T	C	18	GENIC	possibly homozygous	110999415
17	24209174	24209175	T	C	18	GENIC	possibly homozygous	110999417
17	24209193	24209194	C	T	20	GENIC	possibly homozygous	110999419
17	24209327	24209328	A	T	20	GENIC	homozygous	110999421
17	24209661	24209662	G	A	16	GENIC	homozygous	110999423
17	24214196	24214197	A	G	15	GENIC	homozygous	110999427
17	24214379	24214380	C	T	32	GENIC	homozygous	110999429
17	24214493	24214494	C	T	37	GENIC	homozygous	110999431
17	24214703	24214704	G	A	19	GENIC	homozygous	110999433
17	24215459	24215460	A	G	22	GENIC	homozygous	110999435
17	24215919	24215920	C	A	19	GENIC	homozygous	110999437
17	24215977	24215978	A	G	25	GENIC	homozygous	110999439
17	24217174	24217175	G	A	18	GENIC	homozygous	111180593
17	24217219	24217220	T	C	21	GENIC	homozygous	111235173
17	24217279	24217280	C	T	23	GENIC	homozygous	110999443
17	24217287	24217288	T	C	23	GENIC	homozygous	110999445
17	24217311	24217312	T	C	27	GENIC	homozygous	110999447
17	24217356	24217357	G	T	21	GENIC	homozygous	110999449
17	24217485	24217486	G	A	20	GENIC	homozygous	110999451
17	24217559	24217560	T	C	18	GENIC	homozygous	110999453
17	24217932	24217933	T	C	22	GENIC	homozygous	110999455