chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	39620616	39620617	G	A	24	GENIC	homozygous	116763128
10	39620747	39620748	G	A	16	GENIC	homozygous	116763130
10	39620959	39620960	C	T	19	GENIC	homozygous	116763132
10	39620965	39620966	C	T	17	GENIC	homozygous	116870304
10	39620975	39620976	G	A	18	GENIC	homozygous	116763134
10	39620997	39620998	C	T	20	GENIC	homozygous	116763136
10	39621052	39621053	A	G	23	GENIC	homozygous	116763138
10	39621881	39621882	A	G	14	GENIC	homozygous	116763148
10	39621961	39621962	T	C	17	GENIC	homozygous	116763150
10	39621993	39621994	G	A	20	GENIC	homozygous	116763152
10	39622022	39622023	C	T	21	GENIC	homozygous	116763154
10	39622034	39622035	T	C	25	GENIC	homozygous	116763156
10	39622038	39622039	T	C	28	GENIC	homozygous	116763158
10	39622113	39622114	G	T	15	GENIC	homozygous	116763160
10	39622135	39622136	C	T	11	GENIC	homozygous	116763162
10	39622142	39622143	A	G	11	GENIC	homozygous	116763164
10	39622168	39622169	T	C	20	GENIC	homozygous	116763166
10	39622183	39622184	T	C	21	GENIC	homozygous	116763168
10	39622198	39622199	T	C	21	GENIC	homozygous	117076608
10	39622234	39622235	G	A	22	GENIC	homozygous	116763172
10	39622240	39622241	A	G	20	GENIC	homozygous	116763174
10	39622299	39622300	G	A	16	GENIC	homozygous	116763176
10	39622528	39622529	T	C	21	GENIC	homozygous	116763178
10	39622579	39622580	G	A	24	GENIC	homozygous	116763180
10	39622651	39622652	A	G	23	GENIC	homozygous	116870308
10	39622653	39622654	A	C	22	GENIC	homozygous	116870310
10	39622678	39622679	A	G	21	GENIC	homozygous	116763184
10	39622853	39622854	C	T	19	GENIC	homozygous	116763188
10	39622915	39622916	G	A	17	GENIC	homozygous	116870312
10	39622865	39622866	C	T	21	GENIC	homozygous	116567704
10	39622872	39622873	A	T	20	GENIC	homozygous	116567706
10	39622906	39622907	A	G	17	GENIC	homozygous	116567708