chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	36649322	36649323	C	T	20	GENIC	homozygous	117003969
10	36649389	36649390	C	T	32	GENIC	homozygous	116759615
10	36649663	36649664	A	G	37	GENIC	homozygous	116759617
10	36649760	36649761	T	C	26	GENIC	homozygous	116759619
10	36649771	36649772	T	C	26	GENIC	homozygous	117003971
10	36649893	36649894	C	T	24	GENIC	homozygous	116759621
10	36649905	36649906	C	T	23	GENIC	homozygous	116759623
10	36649991	36649992	T	C	30	GENIC	homozygous	116759625
10	36650105	36650106	T	C	35	GENIC	homozygous	116759627
10	36650168	36650169	C	T	27	GENIC	homozygous	116759629
10	36650253	36650254	A	G	28	GENIC	homozygous	116759631
10	36650254	36650255	A	G	29	GENIC	homozygous	116759633
10	36654587	36654588	C	T	31	GENIC	homozygous	116759637
10	36654651	36654652	C	T	22	GENIC	homozygous	116759639
10	36655354	36655355	A	G	25	GENIC	homozygous	116759641
10	36657984	36657985	C	T	21	GENIC	homozygous	116561502
10	36659393	36659394	T	C	30	GENIC	homozygous	116759643
10	36659394	36659395	C	T	30	GENIC	homozygous	116759645
10	36660517	36660518	G	A	31	GENIC	homozygous	116759647
10	36661230	36661231	A	G	20	GENIC	homozygous	116561528
10	36661427	36661428	G	T	26	GENIC	homozygous	116759649