chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	48587556	48587557	C	T	53	GENIC	homozygous	116879995
10	48590150	48590151	A	G	58	GENIC	homozygous	116879997
10	48592193	48592194	T	C	60	GENIC	homozygous	116879999
10	48592498	48592499	T	C	59	GENIC	homozygous	116880001
10	48592783	48592784	C	T	63	GENIC	homozygous	116880003
10	48592866	48592867	T	C	53	GENIC	homozygous	116880005
10	48593591	48593592	C	T	56	GENIC	possibly homozygous	116880007
10	48593708	48593709	T	G	40	GENIC	homozygous	116880009
10	48589124	48589124		GAA	47	GENIC	homozygous	131092888
10	48590657	48590658	A		40	GENIC	homozygous	131092889
10	48594089	48594090	A		34	GENIC	homozygous	131092890
10	48591276	48591277	T	C	51	GENIC	homozygous	117410573
10	48591399	48591400	A		41	GENIC	possibly homozygous	129968926
10	48594111	48594111		GG	26	GENIC	homozygous	131092891
10	48598092	48598093	G	A	62	GENIC	homozygous	116880011
10	48598665	48598666	C	A	65	GENIC	homozygous	116880013
10	48598674	48598675	C	T	71	GENIC	homozygous	116880015
10	48594139	48594140	C	T	25	GENIC	homozygous	117218378