chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	36650551	36650552	T	C	14	GENIC	homozygous	116561490
10	36657463	36657464	A	G	9	GENIC	homozygous	116561494
10	36657506	36657507	A	G	12	GENIC	homozygous	116561496
10	36657770	36657771	G	T	21	GENIC	homozygous	116561498
10	36657771	36657772	G	A	20	GENIC	homozygous	116561500
10	36657984	36657985	C	T	22	GENIC	homozygous	116561502
10	36657996	36657997	A	C	22	GENIC	homozygous	116561504
10	36658070	36658071	G	A	28	GENIC	homozygous	116561506
10	36658143	36658144	T	C	24	GENIC	homozygous	116561508
10	36658225	36658226	A	G	27	GENIC	homozygous	116561510
10	36658265	36658266	G	A	28	GENIC	homozygous	116561512
10	36658580	36658581	A	T	15	GENIC	homozygous	116561514
10	36658793	36658794	G	A	25	GENIC	homozygous	116561516
10	36659199	36659200	T	C	19	GENIC	homozygous	116561518
10	36660202	36660203	A	G	29	GENIC	homozygous	116561520
10	36661052	36661053	A	G	29	GENIC	homozygous	116561522
10	36661097	36661098	T	G	26	GENIC	homozygous	116561526
10	36661230	36661231	A	G	22	GENIC	homozygous	116561528
10	36662604	36662605	C	T	18	GENIC	homozygous	116868505
10	36662748	36662749	G	A	23	GENIC	homozygous	116561530