chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	49368406	49368407	T	C	20	GENIC	homozygous	116882996
10	49369338	49369339	G	A	20	GENIC	homozygous	116882998
10	49371462	49371463	C	G	27	GENIC	homozygous	116883000
10	49371469	49371470	A	G	28	GENIC	homozygous	116883002
10	49377507	49377508	T	G	34	GENIC	homozygous	116883004
10	49378160	49378161	C	T	24	GENIC	homozygous	116883007
10	49378458	49378459	A	T	15	GENIC	homozygous	116883009
10	49378650	49378651	A	G	30	GENIC	homozygous	116883011
10	49381412	49381413	T	A	25	GENIC	homozygous	116883013
10	49382770	49382771	C	T	14	GENIC	homozygous	116883015
10	49383664	49383665	C	T	34	GENIC	homozygous	116883017
10	49383902	49383903	A	G	26	GENIC	homozygous	116883019
10	49383906	49383907	A	C	27	GENIC	homozygous	116883021
10	49390723	49390724	T	C	17	GENIC	homozygous	116883023
10	49391406	49391407	G	A	25	GENIC	homozygous	116883025
10	49393305	49393306	G	A	34	GENIC	homozygous	116883027
10	49394087	49394088	A	G	24	GENIC	homozygous	116883029
10	49394869	49394870	T	C	17	GENIC	homozygous	116883031
10	49394947	49394948	G	C	18	GENIC	homozygous	116883033
10	49395220	49395221	T	G	15	GENIC	homozygous	116883035
10	49395221	49395222	T	A	15	GENIC	homozygous	116883037
10	49395285	49395286	G	T	27	GENIC	homozygous	116883039