chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	15077023	15077024	A	G	46	GENIC	homozygous	110966990
17	15077968	15077969	T	C	28	GENIC	homozygous	110966992
17	15079135	15079136	C	T	35	GENIC	possibly homozygous	110966994
17	15079422	15079423	A	G	33	GENIC	homozygous	110966996
17	15079694	15079695	C	T	28	GENIC	possibly homozygous	110966998
17	15084382	15084383	T	C	30	GENIC	homozygous	110967000
17	15085393	15085394	G	T	30	GENIC	homozygous	110967002
17	15089669	15089670	T	C	61	GENIC	homozygous	110967004
17	15091022	15091023	C	T	38	GENIC	possibly homozygous	110967006
17	15091819	15091820	A	G	32	GENIC	homozygous	110967008
17	15091869	15091870	G	A	34	GENIC	homozygous	110967010
17	15094298	15094299	A	G	43	GENIC	homozygous	110967012
17	15094431	15094432	G	C	29	GENIC	homozygous	110967014