chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	9750011	9750012	C	T	23	GENIC	homozygous	110953011
17	9751454	9751455	T	G	28	GENIC	homozygous	110953013
17	9752802	9752803	T	C	40	GENIC	homozygous	110953015
17	9753215	9753216	T	A	40	GENIC	homozygous	110953017
17	9756364	9756365	T	C	20	GENIC	homozygous	110953019
17	9756995	9756996	T	C	23	GENIC	homozygous	110953021
17	9758439	9758440	C	A	26	GENIC	homozygous	110953023
17	9758877	9758878	T	C	19	GENIC	possibly homozygous	110953025
17	9759701	9759702	C	T	37	GENIC	homozygous	110953027
17	9760253	9760254	A	G	30	GENIC	homozygous	110953029
17	9761051	9761052	G	A	29	GENIC	homozygous	110953031
17	9762177	9762178	T	C	20	GENIC	homozygous	110953033
17	9762414	9762415	T	A	17	GENIC	homozygous	110953035
17	9762500	9762501	C	A	26	GENIC	possibly homozygous	110953037
17	9762557	9762558	T	C	33	GENIC	possibly homozygous	110953039
17	9762680	9762681	A	G	27	GENIC	homozygous	110953041
17	9762691	9762692	C	T	25	GENIC	homozygous	110953043
17	9762721	9762722	T	C	22	GENIC	homozygous	110953045