chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	47577593	47577594	T	C	39	GENIC	homozygous	110336394
18	47578276	47578277	A	T	7	GENIC	homozygous	110336396
18	47578639	47578640	A	G	35	GENIC	homozygous	110336398
18	47578886	47578887	A	C	25	GENIC	homozygous	110471859
18	47578910	47578911	G	A	28	GENIC	homozygous	110336400
18	47579057	47579058	C	T	57	GENIC	homozygous	110336402
18	47579229	47579230	T	C	20	GENIC	homozygous	110336406
18	47579268	47579269	T	C	19	GENIC	homozygous	110336408
18	47579316	47579317	G	A	17	GENIC	homozygous	110336410
18	47586787	47586788	T	C	28	GENIC	homozygous	110336422
18	47588208	47588209	G	A	5	GENIC	homozygous	110336424
18	47590985	47590986	G	A	32	GENIC	homozygous	110336426
18	47591532	47591533	C	A	29	GENIC	homozygous	110336428
18	47594184	47594185	A	G	31	GENIC	homozygous	110336432
18	47594722	47594723	T	C	34	GENIC	homozygous	110336434
18	47595122	47595123	A	C	29	GENIC	homozygous	110336436
18	47596391	47596392	T	G	29	GENIC	possibly homozygous	110336438
18	47596901	47596902	G	A	25	GENIC	homozygous	110336440
18	47597546	47597547	T	C	20	GENIC	homozygous	110336442
18	47598928	47598929	G	A	12	GENIC	homozygous	110336444
18	47603214	47603215	C	T	42	GENIC	homozygous	110336446
18	47584390	47584391	C	T	26	GENIC	homozygous	110533861