chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	4083166	4083167	A	G	35	GENIC	possibly homozygous	110243339
18	4083189	4083190	G	T	35	GENIC	possibly homozygous	110243341
18	4084441	4084442	G	C	38	GENIC	homozygous	110243343
18	4084557	4084558	A	C	37	GENIC	possibly homozygous	110243345
18	4085749	4085750	G	A	23	GENIC	homozygous	110243347
18	4086029	4086030	A	G	50	GENIC	homozygous	119478885
18	4086034	4086035	C	T	51	GENIC	heterozygous	119478886
18	4086052	4086053	G	A	54	GENIC	heterozygous	119478887
18	4086560	4086561	A	G	31	GENIC	homozygous	110243349
18	4087363	4087364	C	T	30	GENIC	homozygous	110243352
18	4087879	4087880	C	T	18	GENIC	homozygous	110243354
18	4088193	4088194	T	C	25	GENIC	homozygous	110243356
18	4088532	4088533	T	C	26	GENIC	homozygous	110243358
18	4088896	4088897	G	A	23	GENIC	homozygous	110243360
18	4089377	4089378	T	C	35	GENIC	homozygous	110243362
18	4089761	4089762	C	G	31	GENIC	heterozygous	119478888
18	4089845	4089846	A	C	24	GENIC	homozygous	110642088
18	4089854	4089855	A	G	27	GENIC	possibly homozygous	110920098
18	4092189	4092190	A	G	55	GENIC	homozygous	110243366
18	4093398	4093399	A	G	49	GENIC	homozygous	110243368
18	4093473	4093474	T	A	45	GENIC	homozygous	110243370
18	4095575	4095576	A	G	29	GENIC	homozygous	110243372
18	4096000	4096001	T	C	36	GENIC	homozygous	110243374
18	4094033	4094034	T	C	17	GENIC	homozygous	110570997