chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	59759032	59759033	C	G	33	GENIC	homozygous	108116355
1	59759423	59759424	G	A	28	GENIC	homozygous	108116356
1	59759560	59759561	T	C	23	GENIC	homozygous	108116357
1	59759748	59759749	T	C	34	GENIC	homozygous	108116358
1	59760068	59760069	A	G	34	GENIC	homozygous	108116359
1	59760170	59760171	A	G	50	GENIC	possibly homozygous	108116360
1	59760188	59760189	T	C	50	GENIC	possibly homozygous	108116361
1	59760266	59760267	C	T	46	GENIC	homozygous	108116362
1	59760397	59760398	G	A	47	GENIC	possibly homozygous	108116363
1	59760492	59760493	A		36	GENIC	homozygous	127388459
1	59760781	59760782	A	G	44	GENIC	homozygous	108116364
1	59761663	59761664	G	C	23	GENIC	heterozygous	108116368
1	59761692	59761693	G	A	27	GENIC	heterozygous	108116369
1	59761701	59761702	C	T	25	GENIC	heterozygous	108116370
1	59761707	59761708	A	G	24	GENIC	heterozygous	108116371
1	59761975	59761976	A	T	29	GENIC	homozygous	108116373
1	59762427	59762428	C	G	43	GENIC	homozygous	108116374
1	59762669	59762670	G	A	33	GENIC	homozygous	108116375
1	59762724	59762725	G	A	35	GENIC	homozygous	108116376
1	59763065	59763066	C	T	29	GENIC	homozygous	108116377
1	59763668	59763669	G	T	42	GENIC	homozygous	108116379
1	59764459	59764460	C	T	41	GENIC	homozygous	108116380
1	59764579	59764580	G	A	48	GENIC	homozygous	108116381
1	59764637	59764638	C	G	53	GENIC	homozygous	108116382
1	59765043	59765044	G	A	37	GENIC	homozygous	108116384
1	59762060	59762061	A		31	GENIC	possibly homozygous	127388460
1	59764036	59764150	TAGATTCCTTTTTGTTTTTTTTTTTCTTTTTCTATTTTTCGGAGCTGGGGACTGAACCCAGGGCCTTGCGCTTGGTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAACCCT		31	GENIC	homozygous	127388461
1	59761668	59761671	TTT		25	GENIC	heterozygous	130518920
1	59761711	59761711		AG	25	GENIC	heterozygous	130518921
1	59761713	59761715	CC		25	GENIC	heterozygous	130518922
1	59764841	59764842	C	A	48	GENIC	possibly homozygous	108116383
1	59765838	59765839	A	G	43	GENIC	homozygous	108116385
1	59766911	59766912	A	C	48	GENIC	homozygous	108116386
1	59767131	59767132	C	T	50	GENIC	homozygous	108116387