chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	48587556	48587557	C	T	29	GENIC	homozygous	116879995
10	48589124	48589124		GAA	29	GENIC	homozygous	131092888
10	48590150	48590151	A	G	17	GENIC	homozygous	116879997
10	48590657	48590658	A		20	GENIC	homozygous	131092889
10	48591276	48591277	T	C	26	GENIC	homozygous	117410573
10	48591399	48591400	A		20	GENIC	homozygous	129968926
10	48592193	48592194	T	C	22	GENIC	homozygous	116879999
10	48592498	48592499	T	C	27	GENIC	homozygous	116880001
10	48592783	48592784	C	T	16	GENIC	homozygous	116880003
10	48592866	48592867	T	C	19	GENIC	homozygous	116880005
10	48593591	48593592	C	T	21	GENIC	homozygous	116880007
10	48593708	48593709	T	G	31	GENIC	possibly homozygous	116880009
10	48594089	48594090	A		16	GENIC	homozygous	131092890
10	48594111	48594111		GG	14	GENIC	homozygous	131092891
10	48594139	48594140	C	T	9	GENIC	homozygous	117218378
10	48598092	48598093	G	A	19	GENIC	homozygous	116880011
10	48598665	48598666	C	A	36	GENIC	homozygous	116880013
10	48598674	48598675	C	T	35	GENIC	homozygous	116880015