chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	59418010	59418011	G	A	21	GENIC	homozygous	113821375
5	59418736	59418737	G	A	19	GENIC	possibly homozygous	113821383
5	59421900	59421901	T	C	25	GENIC	possibly homozygous	113821395
5	59423895	59423896	G	A	16	GENIC	homozygous	113821399
5	59423904	59423905	C	T	15	GENIC	homozygous	113821401
5	59425258	59425259	A	G	8	GENIC	homozygous	113821403
5	59425539	59425540	C	T	13	GENIC	homozygous	113821405
5	59429988	59429989	G	A	32	GENIC	homozygous	113821411
5	59430411	59430412	G	A	19	GENIC	possibly homozygous	113821413
5	59432719	59432720	A	G	24	GENIC	homozygous	113821417
5	59433501	59433502	T	C	21	GENIC	homozygous	113821419
5	59433934	59433935	T	C	23	GENIC	homozygous	113821421
5	59435681	59435682	T	C	11	GENIC	homozygous	113821423
5	59436017	59436018	T	C	18	GENIC	homozygous	113821427
5	59436957	59436958	T	C	16	GENIC	homozygous	113821429
5	59437123	59437124	C	T	17	GENIC	homozygous	113821431
5	59438124	59438125	T	C	15	GENIC	homozygous	113821435
5	59438475	59438476	A	G	12	GENIC	homozygous	113821437
5	59438530	59438531	G	A	10	GENIC	homozygous	113821439
5	59439118	59439119	G	A	22	GENIC	homozygous	113821441
5	59440183	59440184	A	G	23	GENIC	homozygous	113821443
5	59442662	59442663	T	C	40	GENIC	homozygous	113821447
5	59443719	59443720	C	T	15	GENIC	homozygous	113821449
5	59443726	59443727	A	C	13	GENIC	homozygous	113821451
5	59445770	59445771	T	C	15	GENIC	homozygous	113821453
5	59446206	59446207	C	T	23	GENIC	homozygous	113821455