chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	40185745	40185746	A	T	21	GENIC	homozygous	117126466
10	40186688	40186689	C	A	11	GENIC	homozygous	116568737
10	40187014	40187015	C	T	15	GENIC	homozygous	116568739
10	40187280	40187281	T	C	24	GENIC	homozygous	116568743
10	40188517	40188518	T	G	14	GENIC	homozygous	117126468
10	40189422	40189423	A	G	23	GENIC	homozygous	117126470
10	40190178	40190179	T	G	23	GENIC	homozygous	116927434
10	40193434	40193435	C	G	17	GENIC	homozygous	117126472
10	40193509	40193510	A	T	9	GENIC	homozygous	116927438
10	40194533	40194534	T	C	20	GENIC	homozygous	116763930
10	40194580	40194581	A	G	18	GENIC	homozygous	116568745
10	40194724	40194725	A	G	24	GENIC	homozygous	116927444
10	40194752	40194753	T	A	17	GENIC	homozygous	116927446
10	40198277	40198278	A	G	14	GENIC	homozygous	116927450
10	40199912	40199913	C	T	20	GENIC	homozygous	116927452
10	40200581	40200582	A	G	2	GENIC	homozygous	117057557
10	40201342	40201343	A	G	14	GENIC	homozygous	116927454
10	40192113	40192114	A	T	5	GENIC	homozygous	116870414