chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	37652594	37652595	T	C	8	GENIC	homozygous	109694055
19	37652595	37652596	G	T	8	GENIC	homozygous	109694057
19	37652634	37652635	G	C	4	GENIC	homozygous	109694059
19	37653295	37653296	G	C	6	GENIC	homozygous	109694061
19	37654000	37654001	T	C	8	GENIC	homozygous	109961692
19	37654041	37654042	A	C	11	GENIC	homozygous	109694063
19	37655926	37655927	A	G	5	GENIC	homozygous	109694065
19	37657036	37657037	C	T	9	GENIC	homozygous	109694067
19	37658450	37658451	G	A	6	GENIC	homozygous	109694069
19	37658955	37658956	A	T	5	GENIC	homozygous	109924822
19	37659736	37659737	T	C	8	GENIC	homozygous	109694071
19	37659838	37659839	T	A	7	GENIC	homozygous	109694073
19	37659952	37659953	G	T	10	GENIC	homozygous	109694075
19	37660065	37660066	A	G	6	GENIC	homozygous	109694077
19	37660159	37660160	C	T	3	GENIC	homozygous	109694079
19	37660521	37660522	C	T	6	GENIC	homozygous	109694081
19	37660633	37660634	T	C	6	GENIC	homozygous	109694083
19	37660732	37660733	G	A	10	GENIC	homozygous	109694085
19	37660913	37660914	A	G	4	GENIC	homozygous	109694087
19	37662269	37662270	C	A	2	GENIC	homozygous	109694091
19	37662342	37662343	C	G	6	GENIC	homozygous	109694093
19	37662461	37662462	G	A	9	GENIC	homozygous	109694095
19	37663609	37663610	C	A	7	GENIC	homozygous	109694097
19	37663910	37663911	G	A	16	GENIC	homozygous	109694099
19	37664023	37664024	T	G	6	GENIC	homozygous	109694101