chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	135432474	135432475	C	T	29	GENIC	homozygous	136294293
2	135432813	135432814	A	T	37	GENIC	homozygous	136294294
2	135433122	135433123	G	A	39	GENIC	homozygous	136294295
2	135433626	135433626		TG	35	GENIC	homozygous	135944251
2	135433933	135433934	T	C	22	GENIC	homozygous	136294296
2	135435591	135435592	A		20	GENIC	possibly homozygous	135944252
2	135435616	135435617	A	G	22	GENIC	homozygous	136294297
2	135436726	135436726		A	33	GENIC	homozygous	135944253
2	135438031	135438031		AGAGG	4	GENIC	heterozygous	135944255
2	135438949	135439062	AAAAAAATGAAGGAACGGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCACAAGGCCCTGGGTTCGGTCCCCAGCTCCGAAAAAAAGAACCCAAAAAAAAA		31	GENIC	homozygous	135944257
2	135439131	135439132	A	G	38	GENIC	homozygous	136294304
2	135435648	135435649	G	A	19	GENIC	homozygous	136294298
2	135436047	135436048	A	T	30	GENIC	homozygous	136294299
2	135436182	135436183	G	A	39	GENIC	homozygous	136294300
2	135436536	135436537	C	A	41	GENIC	homozygous	136294301
2	135433830	135433834	AAGA		9	GENIC	heterozygous	144580306
2	135436821	135436822	C	T	35	GENIC	homozygous	136294302
2	135437193	135437194	A	G	38	GENIC	homozygous	136294303
2	135439231	135439232	T	C	43	GENIC	homozygous	136294305