chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	45732302	45732303	A	T	19	GENIC	homozygous	116584360
10	45732857	45732858	G	A	24	GENIC	homozygous	116584362
10	45733264	45733265	G	A	20	GENIC	homozygous	116584364
10	45733893	45733894	T	A	16	GENIC	homozygous	116584366
10	45734859	45734860	T	C	38	GENIC	homozygous	116584368
10	45734897	45734898	A	G	39	GENIC	homozygous	116584370
10	45734898	45734899	A	C	40	GENIC	homozygous	116584372
10	45735373	45735374	T	C	27	GENIC	homozygous	116584374
10	45735441	45735442	G	A	24	GENIC	homozygous	116584376
10	45735728	45735729	C	T	29	GENIC	homozygous	116584378
10	45735734	45735735	A	C	31	GENIC	homozygous	116584380
10	45736949	45736950	A	C	28	GENIC	homozygous	116584382
10	45737121	45737122	A	G	26	GENIC	homozygous	116584384
10	45740159	45740160	C	G	28	GENIC	homozygous	116584386
10	45741241	45741242	T	C	42	GENIC	homozygous	116584388
10	45741874	45741875	C	T	31	GENIC	homozygous	116584390
10	45743122	45743123	G	A	28	GENIC	homozygous	116584392
10	45743733	45743734	G	A	12	GENIC	homozygous	117058668
10	45744081	45744082	T	A	26	GENIC	homozygous	116584394
10	45745645	45745646	T	C	43	GENIC	homozygous	116931030
10	45746312	45746313	G	A	22	GENIC	homozygous	116584398