chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	40247747	40247748	G	C	21	GENIC	homozygous	116568879
10	40248280	40248281	C	G	28	GENIC	homozygous	116764008
10	40248287	40248288	A	G	28	GENIC	homozygous	116568883
10	40248300	40248301	C	T	26	GENIC	homozygous	116568885
10	40248480	40248481	C	A	21	GENIC	homozygous	116764010
10	40248587	40248588	C	G	26	GENIC	homozygous	116764012
10	40248638	40248639	C	T	32	GENIC	homozygous	116764014
10	40248938	40248939	T	C	28	GENIC	homozygous	116764016
10	40249115	40249116	C	G	46	GENIC	homozygous	116764018
10	40249700	40249701	T	C	19	GENIC	homozygous	116568889
10	40249947	40249948	T	G	28	GENIC	homozygous	116764020
10	40251240	40251241	G	A	8	GENIC	homozygous	116764022
10	40251529	40251530	T	C	21	GENIC	homozygous	116870428
10	40251735	40251736	A	G	24	GENIC	homozygous	116764024
10	40252051	40252052	C	T	22	GENIC	homozygous	116764026
10	40252066	40252067	T	C	20	GENIC	homozygous	116764028
10	40252934	40252935	T	C	22	GENIC	homozygous	116764030
10	40253038	40253039	T	C	35	GENIC	possibly homozygous	116764032
10	40253450	40253451	C	T	35	GENIC	homozygous	116764034
10	40253751	40253752	T	C	29	GENIC	homozygous	116870430
10	40253991	40253992	T	C	26	GENIC	homozygous	116764036
10	40254191	40254192	A	C	36	GENIC	homozygous	116764038
10	40254347	40254348	A	G	20	GENIC	homozygous	116764040
10	40254376	40254377	G	A	19	GENIC	homozygous	116764042
10	40254433	40254434	A	G	21	GENIC	homozygous	116764044
10	40254710	40254711	T	C	23	GENIC	homozygous	116870432
10	40254874	40254875	C	T	13	GENIC	homozygous	116764046
10	40254993	40254994	G	A	22	GENIC	homozygous	116764048