chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	81296452	81296453	T	TG	19	GENIC	homozygous	61882158
1	81297254	81297255	G	A	18	GENIC	homozygous	62083679
1	81297652	81297653	A	G	33	GENIC	homozygous	61882159
1	81297988	81297989	C	G	42	GENIC	homozygous	61882161
1	81298032	81298033	T	G	44	GENIC	homozygous	62083680
1	81298506	81298507	A	T	14	GENIC	homozygous	62083681
1	81298785	81298786	G	A	19	GENIC	homozygous	62136204
1	81299859	81299860	A	G	31	GENIC	possibly homozygous	61882165
1	81300074	81300075	T	TGTGTGTGTGCGCGCGC	17	GENIC	homozygous	62136205
1	81300141	81300142	T	TCTC	20	GENIC	homozygous	61882166
1	81300791	81300792	G	A	39	GENIC	homozygous	62083683
1	81300848	81300849	G	-	32	GENIC	homozygous	62083684
1	81302256	81302257	G	GAAAAAAAAAAAA	14	GENIC	heterozygous	62136206
1	81302257	81302258	A	-	14	GENIC	heterozygous	62136207
1	81303106	81303107	A	G	41	GENIC	homozygous	61882169
1	81303406	81303407	G	A	45	GENIC	homozygous	62083685
1	81303931	81303932	A	G	23	GENIC	homozygous	62083686
1	81304179	81304180	T	C	13	GENIC	homozygous	61882172
1	81304455	81304456	T	C	30	GENIC	homozygous	62083687
1	81304502	81304511	ATTTTATGG	---------	19	GENIC	homozygous	60746660
1	81305800	81305801	C	T	12	GENIC	homozygous	62136208
1	81305821	81305822	T	TAC	13	GENIC	homozygous	61882174
1	81305981	81305982	C	T	14	GENIC	homozygous	62136209
1	81306341	81306342	T	C	30	GENIC	homozygous	61882175
1	81306352	81306353	G	A	29	GENIC	homozygous	61882176
1	81308125	81308126	A	AC	10	GENIC	homozygous	62136210
1	81309064	81309065	G	A	23	GENIC	homozygous	62083688
1	81309293	81309294	T	C	26	GENIC	homozygous	61882183