chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	126894919	126894920	C	T	36	GENIC	homozygous	114441096
5	126895049	126895050	A	G	35	GENIC	homozygous	114137517
5	126895299	126895300	T	C	21	GENIC	homozygous	114137519
5	126895554	126895555	A	G	17	GENIC	homozygous	114441098
5	126895611	126895612	C	T	20	GENIC	homozygous	114137520
5	126895649	126895650	C	T	16	GENIC	homozygous	114441100
5	126895672	126895673	G	C	15	GENIC	homozygous	114441102
5	126896500	126896501	T	C	36	GENIC	homozygous	113999404
5	126896521	126896522	T	C	33	GENIC	homozygous	113999406
5	126897154	126897155	C	T	25	GENIC	homozygous	114441104
5	126897157	126897158	C	A	25	GENIC	homozygous	113999410
5	126897943	126897944	T	C	35	GENIC	homozygous	113999420
5	126899585	126899586	C	T	24	GENIC	homozygous	114441108
5	126899951	126899952	C	G	17	GENIC	homozygous	113999428
5	126900937	126900938	G	T	35	GENIC	homozygous	114441112
5	126906071	126906072	A	G	20	GENIC	homozygous	113999474
5	126907721	126907722	C	T	11	GENIC	homozygous	114441114
5	126907907	126907908	G	A	16	GENIC	homozygous	114441116
5	126908245	126908246	G	A	28	GENIC	possibly homozygous	113999496
5	126910989	126910990	A	G	23	GENIC	homozygous	114441118