chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	49368406	49368407	T	C	72	GENIC	homozygous	116882996
10	49369338	49369339	G	A	44	GENIC	homozygous	116882998
10	49370350	49370351	G	C	38	GENIC	homozygous	117059188
10	49371462	49371463	C	G	57	GENIC	homozygous	116883000
10	49371469	49371470	A	G	58	GENIC	homozygous	116883002
10	49377507	49377508	T	G	61	GENIC	homozygous	116883004
10	49378160	49378161	C	T	44	GENIC	homozygous	116883007
10	49378458	49378459	A	T	66	GENIC	homozygous	116883009
10	49378650	49378651	A	G	65	GENIC	homozygous	116883011
10	49381412	49381413	T	A	51	GENIC	homozygous	116883013
10	49382770	49382771	C	T	48	GENIC	homozygous	116883015
10	49383664	49383665	C	T	46	GENIC	possibly homozygous	116883017
10	49383902	49383903	A	G	36	GENIC	homozygous	116883019
10	49383906	49383907	A	C	35	GENIC	homozygous	116883021
10	49390723	49390724	T	C	37	GENIC	homozygous	116883023
10	49391406	49391407	G	A	46	GENIC	homozygous	116883025
10	49392243	49392244	G	A	52	GENIC	homozygous	117009410
10	49393305	49393306	G	A	58	GENIC	homozygous	116883027
10	49394087	49394088	A	G	43	GENIC	homozygous	116883029
10	49394869	49394870	T	C	39	GENIC	homozygous	116883031
10	49394947	49394948	G	C	32	GENIC	homozygous	116883033
10	49395220	49395221	T	G	27	GENIC	possibly homozygous	116883035
10	49395221	49395222	T	A	25	GENIC	homozygous	116883037
10	49395285	49395286	G	T	42	GENIC	homozygous	116883039
10	49370338	49370339	G	C	36	GENIC	possibly homozygous	117129814
10	49375246	49375247	C	T	61	GENIC	homozygous	117129816
10	49379307	49379308	C	T	4	GENIC	homozygous	117993804
10	49394978	49394979	C	A	19	GENIC	possibly homozygous	116774471