chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	66601486	66601487	C	T	14	GENIC	homozygous	110702251
2	66601609	66601610	A	T	29	GENIC	homozygous	109801023
2	66601817	66601818	G	A	31	GENIC	homozygous	109801026
2	66601865	66601866	T	C	29	GENIC	homozygous	109801028
2	66607502	66607503	C	A	34	GENIC	heterozygous	109801032
2	66607615	66607616	A	G	33	GENIC	homozygous	109801034
2	66607641	66607642	T	A	39	GENIC	heterozygous	109801036
2	66608250	66608251	C	T	7	GENIC	homozygous	109801040
2	66608281	66608282	G	A	3	GENIC	homozygous	109801042
2	66608422	66608423	T	A	12	GENIC	homozygous	109801046
2	66609062	66609063	C	T	21	GENIC	homozygous	109801047
2	66609082	66609083	T	C	16	GENIC	homozygous	109801049
2	66609367	66609368	A	G	26	GENIC	homozygous	109801051
2	66609909	66609910	G	A	31	GENIC	homozygous	109801053
2	66609949	66609950	C	T	31	GENIC	homozygous	109801055
2	66610365	66610366	C	A	32	GENIC	homozygous	109801057
2	66610386	66610387	T	A	37	GENIC	homozygous	109801059
2	66610772	66610773	A	G	25	GENIC	homozygous	109801061
2	66608897	66608898	G	C	15	GENIC	homozygous	120124539
2	66610781	66610782	T	A	26	GENIC	homozygous	120124540
2	66610813	66610814	G	A	23	GENIC	homozygous	109801063
2	66610843	66610844	T	A	20	GENIC	homozygous	109801065
2	66611307	66611308	G	A	9	GENIC	homozygous	109801067
2	66612267	66612268	A	G	27	GENIC	homozygous	109801084
2	66612376	66612377	A	G	49	GENIC	homozygous	109801086
2	66612537	66612538	C	T	31	GENIC	homozygous	109801088
2	66612981	66612982	C	T	8	GENIC	homozygous	109801090
2	66614326	66614327	G	C	20	GENIC	homozygous	109801101
2	66613043	66613044	C	T	6	GENIC	homozygous	109801091
2	66613628	66613629	G	A	19	GENIC	homozygous	109801095
2	66614565	66614566	A	G	29	GENIC	homozygous	109801103
2	66614606	66614607	A	G	20	GENIC	homozygous	109801105
2	66614928	66614929	A	G	21	GENIC	homozygous	109801107