chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	36650551	36650552	T	C	23	GENIC	possibly homozygous	116561490
10	36651555	36651556	C	T	26	GENIC	homozygous	117989268
10	36654760	36654761	A	G	20	GENIC	homozygous	116561492
10	36657463	36657464	A	G	17	GENIC	homozygous	116561494
10	36657506	36657507	A	G	19	GENIC	homozygous	116561496
10	36657770	36657771	G	T	17	GENIC	homozygous	116561498
10	36657771	36657772	G	A	17	GENIC	homozygous	116561500
10	36657984	36657985	C	T	13	GENIC	homozygous	116561502
10	36657996	36657997	A	C	14	GENIC	homozygous	116561504
10	36658070	36658071	G	A	28	GENIC	homozygous	116561506
10	36658143	36658144	T	C	25	GENIC	homozygous	116561508
10	36658225	36658226	A	G	35	GENIC	homozygous	116561510
10	36658265	36658266	G	A	25	GENIC	homozygous	116561512
10	36658580	36658581	A	T	8	GENIC	homozygous	116561514
10	36658793	36658794	G	A	16	GENIC	homozygous	116561516
10	36659199	36659200	T	C	25	GENIC	homozygous	116561518
10	36660202	36660203	A	G	33	GENIC	homozygous	116561520
10	36661052	36661053	A	G	24	GENIC	homozygous	116561522
10	36661056	36661057	G	A	26	GENIC	homozygous	116561524
10	36661097	36661098	T	G	32	GENIC	homozygous	116561526
10	36661230	36661231	A	G	30	GENIC	homozygous	116561528
10	36662748	36662749	G	A	20	GENIC	homozygous	116561530
10	36663173	36663174	G	C	36	GENIC	heterozygous	117989270