chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	102663617	102663618	A	G	70	GENIC	homozygous	112627216
15	102663865	102663866	C	T	52	GENIC	homozygous	112627218
15	102664452	102664453	G	A	50	GENIC	possibly homozygous	112627220
15	102664989	102664990	G	A	72	GENIC	heterozygous	118933444
15	102665268	102665269	T	C	36	GENIC	homozygous	112627222
15	102665919	102665920	T	C	50	GENIC	homozygous	112627224
15	102666268	102666269	G	T	32	GENIC	possibly homozygous	112627226
15	102666579	102666580	G	A	55	GENIC	homozygous	112627228
15	102667366	102667367	G	A	39	GENIC	possibly homozygous	112627230
15	102667608	102667609	C	A	57	GENIC	possibly homozygous	112627233
15	102667913	102667914	A	G	42	GENIC	homozygous	112627235
15	102668525	102668526	T	C	56	GENIC	homozygous	112627237
15	102669257	102669258	T	C	30	GENIC	homozygous	112627239
15	102670140	102670141	G	T	50	GENIC	homozygous	112627241
15	102670220	102670221	C	T	38	GENIC	homozygous	112627243
15	102670272	102670273	G	A	41	GENIC	homozygous	112627245
15	102670394	102670395	G	A	45	GENIC	homozygous	112627247
15	102670500	102670501	C	T	46	GENIC	homozygous	112627249
15	102670782	102670783	A	G	22	GENIC	homozygous	112627251
15	102670956	102670957	G	A	42	GENIC	homozygous	112627253
15	102666947	102666948	C	T	45	GENIC	homozygous	112763444