chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	34003910	34003911	G	A	21	GENIC	homozygous	116755853
10	34003934	34003935	T	G	21	GENIC	homozygous	116755855
10	34004163	34004164	A	G	35	GENIC	homozygous	116755857
10	34004206	34004207	C	T	33	GENIC	homozygous	116755859
10	34004398	34004399	T	C	26	GENIC	possibly homozygous	116755861
10	34004401	34004402	C	T	24	GENIC	homozygous	117057126
10	34004420	34004421	G	A	29	GENIC	homozygous	116755863
10	34004427	34004428	A	G	29	GENIC	possibly homozygous	116755865
10	34004564	34004565	A	G	21	GENIC	homozygous	116755867
10	34004566	34004567	G	A	21	GENIC	homozygous	116755869
10	34004693	34004694	A	G	19	GENIC	homozygous	116755871
10	34004898	34004899	C	A	17	GENIC	homozygous	116755873
10	34005054	34005055	C	T	19	GENIC	homozygous	116755875
10	34005306	34005307	T	C	13	GENIC	homozygous	116755877
10	34005376	34005377	G	A	18	GENIC	homozygous	116755879
10	34005499	34005500	T	C	16	GENIC	homozygous	116755881
10	34005550	34005551	T	C	11	GENIC	homozygous	116755883