chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	40183394	40183395	A	C	32	GENIC	homozygous	117005371
10	40184151	40184152	G	A	14	GENIC	homozygous	117005379
10	40184513	40184514	G	A	15	GENIC	homozygous	117005383
10	40185090	40185091	C	T	22	GENIC	homozygous	117005385
10	40185126	40185127	C	T	29	GENIC	homozygous	117005387
10	40185328	40185329	G	A	20	GENIC	homozygous	117005389
10	40185555	40185556	C	T	25	GENIC	homozygous	117005391
10	40186688	40186689	C	A	18	GENIC	homozygous	116568737
10	40187014	40187015	C	T	31	GENIC	homozygous	116568739
10	40187023	40187024	C	A	32	GENIC	homozygous	116568741
10	40187280	40187281	T	C	27	GENIC	homozygous	116568743
10	40188252	40188253	T	C	17	GENIC	homozygous	116763922
10	40190416	40190417	C	A	18	GENIC	homozygous	117005397
10	40190614	40190615	C	T	21	GENIC	homozygous	117005399
10	40191428	40191429	G	A	24	GENIC	homozygous	117005401
10	40191446	40191447	T	C	25	GENIC	homozygous	117005403
10	40192113	40192114	A	T	5	GENIC	homozygous	116870414
10	40190178	40190179	T	G	14	GENIC	homozygous	116927434
10	40194167	40194168	C	T	9	GENIC	homozygous	117005409
10	40194533	40194534	T	C	19	GENIC	homozygous	116763930
10	40194580	40194581	A	G	15	GENIC	homozygous	116568745
10	40194724	40194725	A	G	10	GENIC	homozygous	116927444
10	40194881	40194882	C	T	13	GENIC	homozygous	117005411
10	40194975	40194976	G	A	14	GENIC	homozygous	117005413
10	40199569	40199570	T	A	21	GENIC	homozygous	117005415
10	40199887	40199888	G	A	13	GENIC	homozygous	117005417
10	40200422	40200423	C	T	20	GENIC	homozygous	117277750
10	40201342	40201343	A	G	18	GENIC	homozygous	116927454
10	40201352	40201353	A	T	19	GENIC	homozygous	117005419