chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	60619766	60619767	T	G	27	GENIC	homozygous	110757209
18	60619776	60619777	T	C	20	GENIC	homozygous	110757211
18	60619778	60619779	T	C	20	GENIC	homozygous	110757213
18	60619780	60619781	T	C	18	GENIC	homozygous	110757215
18	60619782	60619783	T	C	19	GENIC	homozygous	110757217
18	60620465	60620466	T	C	38	GENIC	homozygous	110369513
18	60620603	60620604	T	C	23	GENIC	possibly homozygous	110369517
18	60621236	60621237	C	T	13	GENIC	possibly homozygous	110757219
18	60621238	60621239	C	T	13	GENIC	possibly homozygous	110757221
18	60621240	60621241	C	T	13	GENIC	possibly homozygous	110757223
18	60621346	60621347	G	A	30	GENIC	homozygous	110757226
18	60624249	60624250	G	A	49	GENIC	possibly homozygous	110757228
18	60624297	60624298	T	A	47	GENIC	possibly homozygous	110757230
18	60624298	60624299	A	T	48	GENIC	possibly homozygous	110757232
18	60625800	60625801	T	C	11	GENIC	homozygous	110369529
18	60626242	60626243	A	T	22	GENIC	possibly homozygous	110757234
18	60626632	60626633	T	C	28	GENIC	homozygous	110369531
18	60626871	60626872	C	T	25	GENIC	homozygous	110757236
18	60627484	60627485	T	C	29	GENIC	homozygous	110369533
18	60628800	60628801	A	G	19	GENIC	homozygous	110369537
18	60631251	60631252	C	T	30	GENIC	possibly homozygous	110757238
18	60631509	60631510	G	A	27	GENIC	homozygous	110757240