chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	8731629	8731630	T	C	45	GENIC	homozygous	113192325
15	8732534	8732535	G	T	52	GENIC	possibly homozygous	113045403
15	8733939	8733940	T	A	40	GENIC	homozygous	113192327
15	8735234	8735234		TTCTTTTC	22	GENIC	heterozygous	131516688
15	8736107	8736108	C	T	64	GENIC	homozygous	113045405
15	8737123	8737124	T	C	35	GENIC	homozygous	113045407
15	8739274	8739276	GT		47	GENIC	homozygous	131516689
15	8739507	8739508	C	T	41	GENIC	homozygous	113045409
15	8740180	8740181	T	C	51	GENIC	homozygous	113045411
15	8743664	8743665	A	G	56	GENIC	homozygous	113192329
15	8744174	8744175	A	G	28	GENIC	homozygous	113192331
15	8744412	8744413	A	T	54	GENIC	homozygous	113045415
15	8744681	8744682	G	C	46	GENIC	homozygous	113192333
15	8749818	8749819	A	G	45	GENIC	homozygous	113192335
15	8750585	8750586	C		53	GENIC	homozygous	131516690
15	8753460	8753461	G	C	46	GENIC	homozygous	113192337
15	8753624	8753625	T	C	37	GENIC	homozygous	113192339
15	8753770	8753771	C	T	40	GENIC	homozygous	113192341
15	8753783	8753784	G	C	40	GENIC	homozygous	113045427
15	8753801	8753802	G	C	41	GENIC	homozygous	113045429
15	8753913	8753914	C	T	56	GENIC	homozygous	113192343
15	8754514	8754515	G	A	40	GENIC	homozygous	113045433
15	8755628	8755629	A	C	33	GENIC	homozygous	113192345