chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	40127992	40127993	A	G	25	GENIC	homozygous	116802086
8	40127995	40127996	C	T	25	GENIC	homozygous	116802088
8	40128059	40128060	A	G	39	GENIC	homozygous	116802090
8	40128457	40128458	G	A	20	GENIC	homozygous	116802092
8	40130195	40130196	A	G	37	GENIC	homozygous	116802094
8	40130619	40130620	C	T	25	GENIC	possibly homozygous	116802096
8	40130629	40130630	A	G	25	GENIC	possibly homozygous	116802098
8	40130932	40130933	G	A	13	GENIC	homozygous	116802100
8	40131031	40131032	C	T	13	GENIC	homozygous	116802102
8	40131110	40131111	T	C	14	GENIC	homozygous	116802104
8	40131468	40131469	C	T	19	GENIC	homozygous	116802106
8	40131701	40131702	C	T	15	GENIC	homozygous	116802108
8	40131800	40131801	G	A	16	GENIC	homozygous	116802110
8	40132061	40132062	T	C	20	GENIC	homozygous	116802112
8	40132402	40132403	A	C	9	GENIC	homozygous	116802114
8	40132690	40132691	C	T	82	GENIC	heterozygous	116802116
8	40133106	40133107	A	T	8	GENIC	heterozygous	116802122
8	40133942	40133943	G	A	30	GENIC	possibly homozygous	116802126
8	40134696	40134697	T	C	35	GENIC	homozygous	116463744
8	40134781	40134782	C	T	15	GENIC	homozygous	116802132
8	40134877	40134878	C	T	20	GENIC	homozygous	116802134
8	40134940	40134941	C	G	27	GENIC	homozygous	116802136
8	40135051	40135052	C	T	19	GENIC	homozygous	116802138
8	40135053	40135054	T	A	19	GENIC	homozygous	116802140
8	40135386	40135387	C	T	22	GENIC	possibly homozygous	116463745
8	40135695	40135696	G	A	23	GENIC	homozygous	116802142
8	40136038	40136039	C	T	27	GENIC	homozygous	116802144
8	40136488	40136489	T	C	16	GENIC	homozygous	116802146
8	40136692	40136693	A	G	13	GENIC	homozygous	116802148
8	40136889	40136890	T	C	27	GENIC	homozygous	116802150
8	40137306	40137307	T	C	19	GENIC	homozygous	116802152