chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	51435359	51435360	C	G	20	GENIC	homozygous	112507241
15	51436476	51436477	C	T	20	GENIC	homozygous	112507243
15	51438610	51438611	A	G	22	GENIC	homozygous	112507245
15	51440537	51440538	C	T	23	GENIC	homozygous	112507247
15	51440864	51440865	A	G	18	GENIC	homozygous	118918614
15	51456014	51456015	C	A	30	GENIC	homozygous	112507249
15	51456070	51456071	G	A	32	GENIC	homozygous	112507251
15	51456844	51456845	G	T	16	GENIC	homozygous	118918616
15	51457249	51457250	C	T	23	GENIC	homozygous	112507253
15	51459576	51459577	T	G	21	GENIC	homozygous	112507255
15	51460342	51460343	G	T	15	GENIC	homozygous	112507257
15	51461080	51461081	A	G	27	GENIC	homozygous	112507259
15	51461224	51461225	G	A	38	GENIC	homozygous	112507261
15	51461259	51461260	A	G	33	GENIC	homozygous	112507263
15	51461962	51461963	C	T	21	GENIC	homozygous	112507265
15	51462532	51462533	C	G	25	GENIC	homozygous	112507267
15	51463287	51463288	G	A	21	GENIC	homozygous	112507269
15	51463737	51463738	A	G	28	GENIC	homozygous	113070660
15	51453746	51453747	G	A	15	GENIC	possibly homozygous	113054309