chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	74137470	74137471	C	G	29	GENIC	homozygous	68063890
10	74138508	74138509	A	G	9	GENIC	homozygous	68063898
10	74139544	74139545	T	A	7	GENIC	homozygous	68656019
10	74141872	74141873	A	G	12	GENIC	homozygous	68063905
10	74143746	74143747	A	G	28	GENIC	homozygous	68063909
10	74143920	74143921	C	T	17	GENIC	homozygous	68656021
10	74145266	74145267	G	C	9	GENIC	homozygous	68063912
10	74146587	74146588	C	T	15	GENIC	homozygous	68063920
10	74146753	74146754	A	T	13	GENIC	homozygous	68656025
10	74146803	74146804	A	G	22	GENIC	homozygous	68063924
10	74150328	74150329	A	C	19	GENIC	homozygous	68063928
10	74151171	74151172	G	T	25	GENIC	homozygous	68063936
10	74154747	74154748	C	A	9	GENIC	possibly homozygous	68063957
10	74155009	74155010	T	C	15	GENIC	homozygous	68656027
10	74155168	74155169	T	C	20	GENIC	homozygous	68063965
10	74159346	74159347	G	T	22	GENIC	homozygous	68063984
10	74164771	74164772	C	G	11	GENIC	homozygous	68063988
10	74164767	74164768	C	G	10	GENIC	homozygous	69192305