chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	100767855	100767856	A	G	20	GENIC	homozygous	120283365
9	100768130	100768131	A	G	8	GENIC	heterozygous	120283366
9	100768556	100768557	G	T	19	GENIC	homozygous	120283367
9	100768647	100768648	A	G	23	GENIC	homozygous	120283368
9	100768780	100768781	C	T	22	GENIC	homozygous	117619911
9	100768815	100768816	C	G	20	GENIC	homozygous	120283369
9	100769715	100769716	A	G	25	GENIC	homozygous	117619913
9	100769841	100769842	T	A	18	GENIC	homozygous	120283370
9	100769915	100769916	C	T	21	GENIC	homozygous	120283371
9	100770169	100770170	G	T	23	GENIC	homozygous	120283372
9	100771475	100771476	G	A	18	GENIC	homozygous	120283373
9	100773814	100773815	T	C	13	GENIC	homozygous	117764300
9	100775192	100775193	C	T	22	GENIC	homozygous	117764304
9	100776672	100776673	T	G	11	GENIC	homozygous	120283377
9	100776800	100776801	G	T	13	GENIC	homozygous	126522597
9	100776825	100776826	A	G	5	GENIC	homozygous	126556280
9	100776947	100776948	C	T	19	GENIC	homozygous	120283378
9	100776983	100776984	T	A	23	GENIC	homozygous	117764306
9	100777660	100777661	C	A	18	GENIC	homozygous	126543891
9	100778702	100778703	C	T	17	GENIC	homozygous	120283379
9	100778733	100778734	C	G	18	GENIC	homozygous	120283380
9	100779052	100779053	C	T	18	GENIC	homozygous	117619923