chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	135431593	135431593		A	53	GENIC	homozygous	146358235
2	135433122	135433123	G	A	54	GENIC	homozygous	136294295
2	135433933	135433934	T	C	38	GENIC	homozygous	136294296
2	135434311	135434312	G	A	35	GENIC	possibly homozygous	141414784
2	135435291	135435292	G	C	51	GENIC	homozygous	141414785
2	135435616	135435617	A	G	50	GENIC	homozygous	136294297
2	135435707	135435708	A	C	40	GENIC	homozygous	141414786
2	135436047	135436048	A	T	46	GENIC	homozygous	136294299
2	135436536	135436537	C	A	45	GENIC	possibly homozygous	136294301
2	135436821	135436822	C	T	41	GENIC	homozygous	136294302
2	135433626	135433626		TG	45	GENIC	homozygous	135944251
2	135435591	135435592	A		37	GENIC	homozygous	135944252
2	135434565	135434567	AG		42	GENIC	homozygous	141332293
2	135438234	135438235	A	T	38	GENIC	homozygous	141414787
2	135438355	135438356	A	T	35	GENIC	homozygous	141414788
2	135438949	135439062	AAAAAAATGAAGGAACGGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCACAAGGCCCTGGGTTCGGTCCCCAGCTCCGAAAAAAAGAACCCAAAAAAAAA		31	GENIC	homozygous	135944257
2	135439131	135439132	A	G	48	GENIC	homozygous	136294304
2	135439231	135439232	T	C	49	GENIC	homozygous	136294305