chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	66601486	66601487	C	T	31	GENIC	homozygous	110702251
2	66601609	66601610	A	T	17	GENIC	homozygous	109801023
2	66601817	66601818	G	A	24	GENIC	homozygous	109801026
2	66601865	66601866	T	C	30	GENIC	homozygous	109801028
2	66601959	66601960	A	G	34	GENIC	homozygous	109801030
2	66607615	66607616	A	G	55	GENIC	homozygous	109801034
2	66608004	66608005	G	C	19	GENIC	homozygous	109801038
2	66608287	66608288	G	A	13	GENIC	homozygous	110702255
2	66608523	66608524	A	G	38	GENIC	homozygous	110702257
2	66609367	66609368	A	G	29	GENIC	homozygous	109801051
2	66611307	66611308	G	A	23	GENIC	homozygous	109801067
2	66611350	66611351	G	T	12	GENIC	homozygous	110702265
2	66611931	66611932	A	C	16	GENIC	homozygous	109801080
2	66612192	66612193	G	A	31	GENIC	homozygous	110702269
2	66612267	66612268	A	G	27	GENIC	homozygous	109801084
2	66614326	66614327	G	C	21	GENIC	homozygous	109801101
2	66614606	66614607	A	G	31	GENIC	homozygous	109801105
2	66614931	66614932	G	T	27	GENIC	homozygous	110702273