chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	40185745	40185746	A	T	31	GENIC	homozygous	117126466
10	40186688	40186689	C	A	23	GENIC	homozygous	116568737
10	40187014	40187015	C	T	23	GENIC	homozygous	116568739
10	40187280	40187281	T	C	31	GENIC	homozygous	116568743
10	40187915	40187916	C	T	27	GENIC	homozygous	118065926
10	40188517	40188518	T	G	38	GENIC	homozygous	117126468
10	40189422	40189423	A	G	24	GENIC	homozygous	117126470
10	40192712	40192712		A	30	GENIC	possibly homozygous	131901725
10	40193434	40193435	C	G	37	GENIC	homozygous	117126472
10	40193713	40193714	G		9	GENIC	homozygous	128809813
10	40190178	40190179	T	G	26	GENIC	homozygous	116927434
10	40193509	40193510	A	T	33	GENIC	homozygous	116927438
10	40193526	40193527	G	A	33	GENIC	homozygous	116927440
10	40192113	40192114	A	T	27	GENIC	homozygous	116870414
10	40192279	40192280	A	C	15	GENIC	homozygous	116977336
10	40192494	40192494		A	26	GENIC	homozygous	128809811
10	40193695	40193696	T		11	GENIC	homozygous	128809812
10	40193732	40193733	C		7	GENIC	homozygous	128809814
10	40193747	40193748	G	C	5	GENIC	homozygous	118081241
10	40194533	40194534	T	C	24	GENIC	homozygous	116763930
10	40194580	40194581	A	G	32	GENIC	homozygous	116568745
10	40194724	40194725	A	G	32	GENIC	homozygous	116927444
10	40194752	40194753	T	A	25	GENIC	homozygous	116927446
10	40195409	40195524	AACACTTAAGATTCTTTTTTTTTTTTTGGTTCTTTTTTTTCGGAACTAGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCAAGCCCC		17	GENIC	homozygous	131091682
10	40195923	40195924	T	C	22	GENIC	homozygous	116763934
10	40198277	40198278	A	G	26	GENIC	homozygous	116927450
10	40198376	40198376		AAC	28	GENIC	homozygous	131901726
10	40199912	40199913	C	T	33	GENIC	homozygous	116927452
10	40201342	40201343	A	G	32	GENIC	homozygous	116927454
10	40193767	40193768	T	A	12	GENIC	homozygous	131905255
10	40200443	40200444	A		20	GENIC	homozygous	132691043
10	40193778	40193778		GAAAAAGAAAAAG	5	GENIC	heterozygous	134226677
10	40199384	40199384		CAA	34	GENIC	possibly homozygous	134226678