chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	102663617	102663618	A	G	29	GENIC	homozygous	112627216
15	102663865	102663866	C	T	13	GENIC	homozygous	112627218
15	102664452	102664453	G	A	19	GENIC	homozygous	112627220
15	102665268	102665269	T	C	16	GENIC	homozygous	112627222
15	102665919	102665920	T	C	30	GENIC	homozygous	112627224
15	102666268	102666269	G	T	8	GENIC	homozygous	112627226
15	102666579	102666580	G	A	21	GENIC	homozygous	112627228
15	102666947	102666948	C	T	15	GENIC	homozygous	112763444
15	102667608	102667609	C	A	19	GENIC	homozygous	112627233
15	102667913	102667914	A	G	18	GENIC	homozygous	112627235
15	102668525	102668526	T	C	24	GENIC	homozygous	112627237
15	102669257	102669258	T	C	28	GENIC	homozygous	112627239
15	102670140	102670141	G	T	36	GENIC	homozygous	112627241
15	102670220	102670221	C	T	33	GENIC	homozygous	112627243
15	102670272	102670273	G	A	17	GENIC	homozygous	112627245
15	102670394	102670395	G	A	19	GENIC	homozygous	112627247
15	102670500	102670501	C	T	24	GENIC	homozygous	112627249
15	102670782	102670783	A	G	36	GENIC	homozygous	112627251
15	102670956	102670957	G	A	25	GENIC	homozygous	112627253