chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	35993028	35993029	G	A	28	GENIC	homozygous	114496943
5	35993517	35993518	T	C	22	GENIC	homozygous	114496945
5	35995201	35995202	G	A	19	GENIC	homozygous	114496947
5	35995609	35995610	T	C	15	GENIC	homozygous	114496949
5	35995869	35995870	G	C	27	GENIC	homozygous	114496951
5	35996376	35996377	C	T	43	GENIC	homozygous	114496953
5	35996991	35996992	A	T	22	GENIC	homozygous	114496955
5	35998972	35998973	T	C	22	GENIC	homozygous	114496957
5	35999553	35999554	G	A	33	GENIC	homozygous	114496959
5	35999594	35999595	C	T	31	GENIC	homozygous	114496961
5	35999682	35999683	A	G	22	GENIC	homozygous	114496963
5	35999935	35999936	C	T	4	GENIC	heterozygous	114496965
5	35999939	35999940	C	T	4	GENIC	heterozygous	114496967
5	36000330	36000331	G	A	40	GENIC	homozygous	114496969
5	36002244	36002245	A	G	21	GENIC	homozygous	114496971
5	36003084	36003085	C	T	21	GENIC	homozygous	114496973
5	36003923	36003924	C	T	25	GENIC	homozygous	114496975
5	36004776	36004777	A	G	48	GENIC	possibly homozygous	114496977
5	36005343	36005344	T	C	27	GENIC	homozygous	114496979
5	36005905	36005906	A	G	19	GENIC	homozygous	114496981
5	36007783	36007784	A	C	48	GENIC	homozygous	113742239
5	36008384	36008385	G	A	56	GENIC	possibly homozygous	114496983
5	36008441	36008442	A	G	43	GENIC	homozygous	113742241
5	36010576	36010577	G	C	29	GENIC	homozygous	114496985
5	36010682	36010683	G	A	34	GENIC	homozygous	114496987
5	36015146	36015147	A	G	21	GENIC	homozygous	113742253
5	36015231	36015232	G	A	17	GENIC	homozygous	114496989
5	36017439	36017440	T	G	13	GENIC	homozygous	114496991
5	36017942	36017943	A	C	21	GENIC	homozygous	113742255