chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	90958090	90958091	A	AG	36	GENIC	homozygous	51538783
10	90958103	90958104	C	G	42	GENIC	homozygous	51738333
10	90958873	90958874	A	G	59	GENIC	possibly homozygous	51738335
10	90959547	90959548	C	G	57	GENIC	homozygous	51738337
10	90959548	90959549	C	T	56	GENIC	homozygous	51738339
10	90959588	90959589	A	G	53	GENIC	homozygous	51738341
10	90959673	90959683	TGGGGACGTT	----------	25	GENIC	homozygous	51738343
10	90959727	90959728	A	G	40	GENIC	homozygous	51738346
10	90961676	90961677	A	C	55	GENIC	homozygous	51738348
10	90962261	90962262	A	G	54	GENIC	possibly homozygous	51738350
10	90963005	90963006	C	G	57	GENIC	possibly homozygous	51738352
10	90963374	90963375	G	C	48	GENIC	homozygous	51738354
10	90964011	90964018	GAAAAGA	-------	13	GENIC	homozygous	51538784
10	90964012	90964016	AAAA	----	13	GENIC	homozygous	51538785
10	90964033	90964034	G	GT	16	GENIC	heterozygous	51738356
10	90964037	90964038	T	-	17	GENIC	heterozygous	51538786
10	90964045	90964046	T	TGTGC	13	GENIC	possibly homozygous	51738358
10	90964062	90964063	T	G	21	GENIC	homozygous	51538787
10	90964318	90964319	C	T	61	GENIC	homozygous	51738360
10	90964463	90964464	T	TAA	30	GENIC	homozygous	51738362
10	90964518	90964525	GGGGTTC	-------	22	GENIC	homozygous	51738364
10	90965014	90965016	TG	--	10	GENIC	homozygous	51738366
10	90965599	90965600	A	G	55	GENIC	heterozygous	51738368
10	90965616	90965617	T	C	44	GENIC	heterozygous	51738370
10	90965616	90965617	T	TAC	22	GENIC	possibly homozygous	51738372
10	90966366	90966367	T	-	3	GENIC	homozygous	51738374
10	90966431	90966432	C	CT	31	GENIC	heterozygous	51538788
10	90967951	90967952	T	G	39	GENIC	homozygous	51538789
10	90966431	90966432	C	CTT	31	GENIC	possibly homozygous	51738376
10	90966997	90966998	A	-	44	GENIC	homozygous	51738378
10	90968077	90968078	A	G	76	GENIC	homozygous	51738381