chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	48603673	48603674	C	G	32	GENIC	homozygous	112503078
15	48608014	48608015	G	T	39	GENIC	homozygous	118916530
15	48610808	48610809	G	C	30	GENIC	homozygous	112503080
15	48611797	48611798	A	G	26	GENIC	homozygous	112503082
15	48612687	48612688	T	C	47	GENIC	homozygous	112503084
15	48632965	48632966	G	C	31	GENIC	homozygous	112503086
15	48633603	48633604	A	T	25	GENIC	homozygous	112503088
15	48634841	48634842	G	T	19	GENIC	heterozygous	118916531
15	48642432	48642433	G	A	42	GENIC	homozygous	112503090
15	48642433	48642434	G	A	40	GENIC	homozygous	112503092
15	48642549	48642550	C	T	28	GENIC	homozygous	112503094
15	48644179	48644180	A	T	22	GENIC	homozygous	112503096
15	48648833	48648834	T	C	9	GENIC	heterozygous	112503098
15	48650610	48650611	G	T	22	GENIC	possibly homozygous	113170947
15	48653348	48653349	G	T	51	GENIC	homozygous	112503100
15	48656007	48656008	T	C	26	GENIC	heterozygous	118916532
15	48656719	48656720	A	C	33	GENIC	homozygous	112503102
15	48656874	48656875	C	G	27	GENIC	homozygous	112503104
15	48658635	48658636	C	T	34	GENIC	homozygous	112503108
15	48658862	48658863	C	T	26	GENIC	homozygous	112503110
15	48659492	48659493	C	A	63	GENIC	heterozygous	118916533
15	48659528	48659529	C	T	70	GENIC	heterozygous	118916534
15	48660024	48660025	C	T	42	GENIC	homozygous	112503112
15	48660478	48660479	G	C	11	GENIC	possibly homozygous	112503114
15	48661289	48661290	C	T	35	GENIC	possibly homozygous	112503116
15	48661476	48661477	G	C	16	GENIC	homozygous	112503117
15	48664277	48664278	A	G	44	GENIC	heterozygous	118916535
15	48665545	48665546	C	T	31	GENIC	homozygous	112503121
15	48667044	48667045	G	A	21	GENIC	homozygous	112503125
15	48667932	48667933	G	T	9	GENIC	homozygous	118916536
15	48668581	48668582	G	T	13	GENIC	homozygous	112503127
15	48668598	48668599	G	A	7	GENIC	homozygous	112503129
15	48668640	48668641	G	T	5	GENIC	homozygous	112809042